Hyperfine Inc (HYPR)

Hyperfine Announces European Launch of Next-Generation Swoop® SystemJuly 1, 2026 8:15 AM
Business Wire Hyperfine has initiated the launch of the next-generation Swoop® system in European markets, beginning the global expansion of its most advanced portable MRI technology. Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced the European launch of the next-generation Swoop® system powered by the latest advancement in Optive AI™ software. This marks a significant milestone in the company’s global expansion of its most advanced portable MRI technology, supporting international commercial growth and improving global access to high-quality brain imaging at the point of care. Following CE mark and UKCA approval, the next-generation Swoop® system, also known as Model 2, is now commercially available across an initial wave of European markets. Professor Steve Williams, Professor of Neuroimaging at King’s College London and Head of the Department of Neuroimaging at the Institute of Psychiatry, Psychology & Neuroscience, commented, "I've been involved with Hyperfine since the earliest days of portable MRI, and the relentless progress has been remarkable. With the next-generation Swoop® system, the improvement in image quality is transformative. Having spent my career exploring advanced brain imaging, I am impressed that low-field MRI can provide this level of diagnostic-quality images. For years, limited access to neuroimaging has delayed diagnosis and treatment for countless patients around the world. The Swoop® system is uniquely positioned to address that gap, making MRI accessible when and where it is needed, even in remote locations, to support decision-making in a wider range of care settings across the lifespan." Hyperfine also announced the inclusion of its next-generation Swoop® system (Model 2) in the UniHA procurement listing, a key milestone enabling broader adoption across hospitals within the French public healthcare system. The initial inclusion of the Swoop® system in this listing was in October 2025. “We are proud to bring Hyperfine’s most advanced portable MRI technology to clinicians across Europe and the UK, delivering on an important milestone for our commercialization strategy in 2026,” said Eric Willis, Vice President of International at Hyperfine. “The next-generation system delivers significant improvements in image quality, workflow efficiency, and clinical capability. We have already seen these advancements accelerate use and adoption of the Swoop® system throughout the United States. We look forward to working closely with our distribution partners to expand access to AI-powered portable MRI across Europe, providing critical neuroimaging that helps clinicians make more timely and more informed patient care decisions. By the end of the year, we plan to make the Model 2 Swoop® system available through our distribution partners across all European markets where Hyperfine is represented.” The European commercial launch adds to Hyperfine’s recent corporate momentum, including its inclusion in the Russell 2000® Index, as the company continues to expand global access to its AI-powered portable MRI technology. For more information about the Swoop® system, please visit HyperfineMRI.com. About the Swoop® Portable MRI Systems
The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. About Hyperfine, Inc.
Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com. Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine. Forward-Looking Statements
This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future ; the inability of the Company to progress on product advancements and improvements ; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. View source version on businesswire.com: https://www.businesswire.com/news/home/20260701134409/en/ Media Contact
Devin Zell
Hyperfine
dzell@hyperfine.io Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine Announces European Launch of Next-Generation Swoop® System

Hyperfine Forms Global Neurosurgery Advisory Council to Support Expansion of Portable MRI in Neurosurgical CareJune 22, 2026 8:15 AM
Business Wire Leading neurosurgeons from around the world will help guide the role of the Swoop® system in neurosurgical care, including surgical workflow, product capabilities, and clinical evidence. Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced the formation of its Neurosurgery Advisory Council, a multidisciplinary group of leading neurosurgeons who will provide expertise to help inform the potential role of portable ultra-low-field MRI in neurosurgical applications and shape the future of imaging in neurosurgical care. “The neurosurgical setting is becoming an important site of care for accessible imaging, where traditional MRI has intrinsic limitations. The Swoop® system may open up new possibilities for integrating imaging directly into surgical workflows,” said Hyperfine Chief Operating Officer Tom Teisseyre. “Providing access to imaging at key moments around a procedure may help clinical teams make better informed decisions, improve efficiency, and ultimately advance how surgical care is delivered.” The Neurosurgery Advisory Council brings together distinguished neurosurgeons from leading academic medical centers and community hospitals around the world, representing expertise in craniotomy, endovascular neurosurgery, transsphenoidal surgery, tumor resection, and other complex procedures. Together, members will help evaluate the potential role of the Swoop® system across the neurosurgical continuum—from preoperative planning and intraoperative decision-making to postoperative monitoring and discharge. The council will provide strategic clinical guidance on workflow integration, product development, and evidence generation while sharing real-world experience that may help define best practices and expand the clinical utility of portable MRI across neurosurgical subspecialties. “The neurosurgical community has long recognized the value of intraoperative MRI, but access has been limited by the substantial infrastructure requirements, cost, and workflow demands of having a high-field MRI system in the OR,” said Edmond Knopp, MD, Chief Medical Officer of Hyperfine. “Portable, ultra-low field MRI has the potential to fundamentally change how and where imaging is used throughout the neurosurgical care pathway. Through collaboration with leading experts in the field, we aim to accelerate its integration into clinical practice and maximize its impact on surgical decision-making and patient care.” The initial members include: Hakan Emmez, MD, PhD
Professor of Neurosurgery
Güven Hospital
(Ankara, Turkey) Brian Jankowitz, MD
Chief of Neurosurgery
JFK University Medical Center
(Edison, New Jersey, USA) Elad I. Levy, MD, MBA, FCNS
Professor and Chair
University at Buffalo Neurosurgery
(Buffalo, New York, USA) G. Michael Lemole, Jr, MD, MBA, FAANS, FACS
Neurosurgeon (Skull Base and Cranial Surgery) at Jefferson Abington Hospital
Professor, Department of Neurological Surgery at Thomas Jefferson University
(Abington, Pennsylvania, USA) Debraj "Raj" Mukherjee, MD, MPH
Associate Professor and Assistant Residency Program Director
Department of Neurosurgery
Johns Hopkins Medical Institutions
(Baltimore, Maryland, USA) Todd Patrick, MD, PhD
Chief of Neurosurgery
Christus Trinity Mother Frances Health System
(Tyler, Texas, USA) Michael Schulder, MD, FAANS
Professor and Vice Chairman, Department of Neurosurgery
Zucker School of Medicine at Hofstra/Northwell
(Manhasset, New York, USA) Adnan Siddiqui, MD, PhD, FAHA
Vice-Chairman and Professor of Neurosurgery
Jacobs School of Medicine & Biomedical Sciences
(Buffalo, New York, USA) Julian Spears, MD, SM, FRCS(C), FACS
Head, Division of Neurosurgery
Chair in Brain Tumor and Cerebrovascular Surgery
St. Michael’s Hospital, Unity Health Toronto
Department of Surgery, University of Toronto
(Toronto, Ontario, Canada) By convening leading neurosurgeons across subspecialties and care settings, Hyperfine aims to accelerate evaluation of portable MRI in neurosurgical workflows and help expand the clinical utility of the Swoop® system in this important area of care. For more information about the Swoop® system, please visit HyperfineMRI.com. About the Swoop® Portable MRI Systems The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. About Hyperfine, Inc. Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com. Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine. Forward-Looking Statements This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future ; the inability of the Company to progress on product advancements and improvements ; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. View source version on businesswire.com: https://www.businesswire.com/news/home/20260622808552/en/ Media Contact
Devin Zell
Hyperfine
dzell@hyperfine.io Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine Forms Global Neurosurgery Advisory Council to Support Expansion of Portable MRI in Neurosurgical Care

How high will HYPR go June 26 at the close?? Russell 2000 & 3000 index add for HYPR happens. Obviously front runners were buying yesterday ... 4 milllion+ shares. They will make money. How high is high for a thinly traded microcap? Gap down from $2 still needs to finish filling ... 1.94 to 2.

Hyperfine Swoop® System Scan Volume in the United States Hits Record Milestones Across Multiple Sites of CareJune 18, 2026 8:15 AM
Business Wire Routine clinical use is accelerating, driven by advanced image quality, expanding clinical utility, and increasingly diverse use cases across hospital and office settings. Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced the achievement of scan volume milestones in key hospitals and neurology clinics, demonstrating accelerating clinical utilization and adoption of the Swoop® system throughout the United States. The increasing clinical use of the Swoop® system is driven by several factors: enhanced clinical utility from improved image quality, growing evidence of its economic value, and expanding adoption across new care settings, including neurology clinics and the emergency department (ED). The most successful Swoop® system programs are driven by visionary healthcare leaders who are passionate about addressing the challenges of MRI availability and recognize the clinical and economic value of portable MRI in expanding patient access to imaging. Jennifer Villa Frabizzio, MD, Chief of Neuroradiology at Jefferson Abington Hospital, who has used the Swoop® system for over three years, commented, “We are excited to have surpassed one thousand Swoop® system scans, making us the highest volume center in the United States. Since we have such a robust Swoop® system program, we decided to evaluate the impact to our hospital, which was recently published in a peer-reviewed journal. We were impressed to find that increasing access to imaging with the Swoop® system not only improved patient care but also delivered meaningful cost savings, significantly reduced MRI wait times in the ICU and ED, and improved patient progression throughout the hospital. Recently, we have also started using the Swoop® system for outpatient brain MRI to reduce wait times for patients at outpatient clinics.” As healthcare systems face mounting pressure to improve both efficiency and quality of care, Jefferson Abington's experience provides compelling evidence that portable brain MRI offers strong clinical utility and a favorable health economic profile, particularly at scale. CHRISTUS Mother Frances, one of the first sites to adopt the next-generation Swoop® system, crossed the 500-scan milestone in just nine months, driven by integrating the Swoop® system into a scalable stroke program. As adoption continues to accelerate, Chief Medical Officer at the center, Mark Anderson, MD, shared, “The Swoop® system has had such a big impact improving patient care and hospital efficiency with our stroke patients in the main hospital ED, we purchased an additional system to place in a satellite ED to help triage stroke patients – enabling faster patient care and avoiding unnecessary admissions and transport costs. We are also pioneering use in the operating room, becoming the first in the United States to conduct transsphenoidal tumor resection using the Swoop® system pre- and post-operatively to confirm surgical success.” Clinical use of the Swoop® system is accelerating in neurology offices, where it has quickly become a valuable extension of the diagnostic workflow since its introduction in mid-2025. Neurology of Central Florida has already exceeded 500 in-office MRI scans, demonstrating how point-of-care imaging enables neurologists to complete diagnostic evaluations within their own practice. As Alicia Cabrera, MD, noted, “The Swoop® System is an excellent tool to expedite the diagnostic process—it’s the missing link we didn’t have before. Patients used to wait weeks for imaging and results; now we can often get answers within 24 to 72 hours, allowing faster decisions and helping avoid unnecessary emergency room visits.” The Swoop® system provides a more comfortable and convenient patient experience, supported by NEURO PMR findings showing a 4:1 patient preference for portable MRI. It is now routinely used for outpatient applications, including headache, dementia, multiple sclerosis surveillance, and emerging brain health assessments. “The experiences at Jefferson Abington, CHRISTUS Mother Frances, and Neurology of Central Florida reflect what we hear consistently from clinicians—timely access to MRI remains a meaningful challenge and portable MRI is helping address that need,” said Maria Sainz, President and CEO of Hyperfine. “By eliminating the barriers that have long defined conventional MRI—wait times, technologist shortages, cost, and immobility—the Swoop® system enables faster decision-making across the hospital and beyond. At Hyperfine, we have redefined what MRI delivery looks like, and we remain committed to supporting brain health by making high-quality imaging available to more patients across more care settings.” Hear more from these hospital centers in our recent webinar on how portable MRI is transforming stroke care. For more information about the Swoop® system, please visit HyperfineMRI.com. About the Swoop® Portable MRI Systems
The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. About Hyperfine, Inc.
Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com. Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine. Forward-Looking Statements
This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future ; the inability of the Company to progress on product advancements and improvements ; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. View source version on businesswire.com: https://www.businesswire.com/news/home/20260618936203/en/ Media Contact
Devin Zell
Hyperfine
dzell@hyperfine.io Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine Swoop® System Scan Volume in the United States Hits Record Milestones Across Multiple Sites of Care

More solid new from HYPR from a few days ago. TA looks strong. Front runners will take HYPR higher going into the Russell 2000 and 3000 index add for HYPR. That's huge for HYPR. Indexes very likely to buy higher. June 26 after market and the coming months should be great for HYPR longs IMO. And HYPR presents next Thursday at an investor conference. Eager to see the updated presentation. https://finance.yahoo.com/sectors/healthcare/articles/hyperfine-announces-presentation-results-prime-121500780.html

Hyperfine shares rise after expected Russell index addition (HYPR)May 26, 2026 8:57 AM
IH Market News Shares of Hyperfine (NASDAQ:HYPR) gained 4% in premarket trading on Tuesday after the company announced that it is expected to be added to both the Russell 3000 Index and the Russell 2000 Index. Russell inclusion set to take effect after June reconstitution The medical technology company said its inclusion is expected to occur as part of the June 2026 Russell index reconstitution process, based on a preliminary list published by FTSE Russell on May 22, 2026. The changes are scheduled to become effective following the close of U.S. trading on June 26, 2026. Russell indexes track largest U.S. listed companies The annual Russell U.S. index reconstitution ranks up to 4,000 of the largest publicly traded American companies based on total market capitalization as of April 30. Companies included in the Russell 3000 Index are automatically assigned to either the large-cap Russell 1000 Index or the small-cap Russell 2000 Index. Russell indexes are widely followed by institutional investors and asset managers, serving as benchmarks for both index-tracking funds and actively managed investment strategies. According to FTSE Russell data, approximately $12.2 trillion in assets were benchmarked against Russell U.S. indexes as of the end of June 2025. Hyperfine continues expansion of portable MRI platform Hyperfine develops the Swoop portable MRI system, described as the first FDA-cleared AI-powered portable MRI platform for brain imaging. The system is designed to enable MRI imaging across multiple points of care and clinical settings. CEO says inclusion reflects commercial progress Maria Sainz, President and Chief Executive Officer of Hyperfine, said the company’s anticipated Russell index inclusion highlights ongoing execution of its commercial growth strategy and rising awareness of its portable MRI technology. Hyperfine stock price Original: Hyperfine shares rise after expected Russell index addition (HYPR)

Hyperfine to Join Russell 2000® and Russell 3000® IndexesMay 26, 2026 8:15 AM
Business Wire Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system— today announced that Hyperfine is expected to join the broad-market Russell 3000® Index and the small-cap Russell 2000® Index at the conclusion of the June 2026 Russell Reconstitution, according to a preliminary list of additions posted by FTSE Russell on May 22, 2026. Hyperfine's inclusion will become effective after the U.S. market close on June 26, 2026. The June reconstitution of the Russell US indexes captures up to the 4,000 largest U.S. stocks as of April 30, ranking them by total market capitalization. Membership in the Russell 3000® Index, which remains in place for six months under the semi-annual reconstitution schedule beginning in 2026, means automatic inclusion in the large-cap Russell 1000® Index or small-cap Russell 2000® Index as well as the appropriate growth and value style indexes. FTSE Russell determines membership for its Russell indexes primarily by objective, market-capitalization rankings and style attributes. “We are pleased that Hyperfine is expected to join the Russell 3000 and Russell 2000 Indexes as part of the June 2026 reconstitution,” said Maria Sainz, President and Chief Executive Officer of Hyperfine. “We believe this inclusion reflects the continued progress in executing our commercial strategy, broadening awareness and driving adoption of our portable MRI technology and creating long-term value for shareholders.” Russell indexes are widely used by investment managers and institutional investors for index funds and as benchmarks for active investment strategies. According to data as of the end of June 2025, about $12.2 trillion in assets are benchmarked against the Russell US indexes, which belong to FTSE Russell, the global index provider. About the Swoop® Portable MRI Systems
The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. About Hyperfine, Inc.
Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com. Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine. Forward-Looking Statements
This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future; the inability of the Company to progress on product advancements and improvements; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. View source version on businesswire.com: https://www.businesswire.com/news/home/20260526952799/en/ Media Contact
Devin Zell
Hyperfine
dzell@hyperfine.io Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine to Join Russell 2000® and Russell 3000® Indexes

Hyperfine Announces Presentation of Results from the PRIME Study Showing Portable MRI Substantially Reduces Time to Imaging in Emergency DepartmentsMay 22, 2026 8:15 AM
Business Wire Prospective randomized ED study shows rapid bedside imaging, detection of critical neurological findings, and potential workflow efficiency benefits with portable MRI Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced the presentation of results of the PRIME (Portable Rapid Imaging for Medical Emergencies) study at the Society for Academic Emergency Medicine (SAEM) 2026 Annual Meeting. PRIME is a single-center, prospective, randomized controlled trial designed to evaluate the role of portable MRI in neurological emergencies in the emergency department (ED), including the technology’s potential effectiveness and efficiency in supporting triage decisions for a wide range of brain-related emergency medical conditions. Conducted at a tertiary emergency department, the study enrolled 100 participants and compared standard clinical workflow using conventional MRI, along with a care pathway that incorporated a portable MRI system at the patient’s bedside. Results presented at SAEM demonstrate a significant reduction in time to imaging for patients randomized to the portable MRI arm. Median time from imaging order to scan start was 1.28 hours in the portable MRI group, compared with 7.76 hours in the conventional MRI only control arm—a median difference of 6.35 hours. 18.6% of the scans completed revealed critical pathology, including acute ischemic stroke, mass lesions, mass effect, and hydrocephalus, all of which were successfully detected by portable MRI and confirmed on conventional MRI. “These findings suggest that portable MRI can be integrated into emergency department workflow far more quickly than conventional MRI and can provide clinically meaningful information when time matters most,” said Dr. Charles Wira, Associate Professor of Emergency Medicine at Yale University. “By bringing advanced imaging to the bedside, portable MRI has the potential to improve diagnostic efficiency, reduce delays, and support faster treatment decisions for patients with neurological emergencies.” “Portable MRI also has the potential to meaningfully reduce emergency department boarding by helping to alleviate delays associated with waiting for access to conventional MRI,” said Dr. Kevin Sheth, Professor of Neurology and Neurosurgery at the Yale School of Medicine and principal investigator for the PRIME study. “Reducing imaging-related bottlenecks may help ED teams move patients through care pathways more efficiently while maintaining access to advanced neuroimaging.” The PRIME study builds on prior research evaluating portable MRI in emergency settings and expands the evidence base by studying a broader emergency department population. PRIME was conducted using the Hyperfine Model 2 Swoop® portable MRI system powered by Optive AI™ software, which is designed to deliver sharper anatomical detail and support broader use of portable brain imaging across emergency care environments. “Enrollment in PRIME was very fast, signaling how frequently MRI is needed as a triage tool in the ED. The presentation of these data at SAEM represents an important milestone for Hyperfine and for the future of emergency neuroimaging,” said Maria Sainz, President and CEO of Hyperfine. “We believe these results reinforce the potential for portable MRI to help clinicians access actionable imaging information sooner, improve emergency department workflows for ruling in and ruling out pathology, and expand access to advanced brain imaging where conventional MRI remains difficult to obtain.” Hyperfine is committed to advancing the role of portable MRI in emergency care, where timely access to conventional MRI remains a challenge for many hospitals. The PRIME study adds to a growing body of evidence supporting portable MRI as an efficient adjunct to emergency neuroimaging and underscores its potential to reduce diagnostic delays and improve patient care at the point of care. For more information about the Swoop® system, please visit HyperfineMRI.com. About the Swoop® AI-Powered Portable MRI Systems The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. About Hyperfine, Inc. Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com. Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine. Forward-Looking Statements This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop ® system is accepted and used by healthcare professionals; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future ; the inability of the Company to progress on product advancements and improvements ; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. View source version on businesswire.com: https://www.businesswire.com/news/home/20260522721021/en/ Media Contact
Devin Zell
Hyperfine
dzell@hyperfine.io Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine Announces Presentation of Results from the PRIME Study Showing Portable MRI Substantially Reduces Time to Imaging in Emergency Departments

Hyperfine, Inc. Reports First Quarter 2026 Financial ResultsMay 12, 2026 4:05 PM
Business Wire Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable magnetic resonance (MR) brain imaging system—the Swoop® system—today announced first quarter 2026 financial results and provided a business update. “Our execution in Q1 was strong. We delivered our second-highest revenue quarter to date with over 80% year-over-year revenue growth, driven by our accelerating commercial engine. We believe the international regulatory clearances we secured, the clinical data we released to the neurology and stroke communities, and the continued momentum in our office and hospital businesses all indicate portable brain MRI is becoming mainstream, and we are leading the charge,” said Maria Sainz, Chief Executive Officer and President of Hyperfine, Inc. Recent Achievements and Business Highlights Obtained CE Marking and UK Conformity Assessment (UKCA) approval for both the next-generation Swoop® system and the latest Optive AI™ software in Europe. Enrolled first patient in Contrast PMR, a study designed to support a future FDA 510(k) submission to expand the Swoop® system’s intended use to include gadolinium-based contrast agents; enrollment currently is over 50% of target. Presented NEURO-PMR results at the 2026 American Society of Neuroimaging showing high diagnostic value and superior patient experience in neurology clinics. Published paper in Stroke: Vascular and Interventional Neurology (SVIN) demonstrating the Swoop® system’s enhanced stroke detection capabilities. Published paper in Clinical Neuroimaging demonstrating the significant health economic benefit of using the Swoop® system. Began launch activities in India market with first Swoop® system live in clinical use at All India Institute of Medical Sciences (AIIMS), New Delhi. Bolstered balance sheet through $15.0 million debt financing, extending the expected cash runway into 2028, and providing capital for commercial growth. First Quarter 2026 Financial Results Revenues for the first quarter of 2026 were $3.90 million, increasing 83% compared to $2.14 million in the first quarter of 2025. Sold 10 commercial Swoop® systems in the first quarter of 2026, compared to six in the first quarter of 2025. Gross profit for the first quarter of 2026 was $1.98 million, compared to $0.88 million in the first quarter of 2025, representing 51% gross margin in the first quarter of 2026, compared to 41% gross margin in the first quarter of 2025. Research and development expenses for the first quarter of 2026 were $3.85 million, decreasing 24% compared to $5.04 million in the first quarter of 2025. Sales, marketing, general, and administrative expenses for the first quarter of 2026 were $6.69 million, compared to $6.75 million in the first quarter of 2025. Net loss for the first quarter of 2026 was $8.62 million, equating to a net loss of $0.09 per share, as compared to a net loss of $9.42 million, or a net loss of $0.12 per share, for the first quarter of 2025. The first quarter of 2026 net loss includes a $0.24 million loss from a change in the fair value of warrant liabilities, compared to a $1.62 million gain in the first quarter of 2025. 2026 Financial Guidance Management continues to expect revenue for the full year 2026 to be approximately $20 to $22 million, representing 55% growth at the midpoint as compared to full year 2025. Management continues to expect cash burn1 for the full year 2026 to be approximately $26 to $28 million, representing a 10% decline at the midpoint as compared to full year 2025. 1Cash burn is calculated as change in cash and cash equivalents less net financing proceeds. Conference Call Hyperfine, Inc. will host a conference call at 1:30 p.m. PT/ 4:30 p.m. ET on Tuesday, May 12, 2026 to discuss its first quarter 2026 financial results and provide a business update. Those interested in listening should register online by visiting https://investors.hyperfine.io/ and clicking on News & Events. Participants are encouraged to register more than 15 minutes before the start of the call. A live and archived audio webcast will be available through the Investors page of Hyperfine, Inc.’s corporate website at https://investors.hyperfine.io/. About Hyperfine, Inc. and the Swoop® Portable MR Imaging® Systems Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first U.S. Food and Drug Administration (FDA)-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit hyperfine.io. The Swoop® Portable MR Imaging® systems are FDA cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. The Swoop® system also has CE Mark in the European Union and UKCA Mark in the United Kingdom. The Swoop® system is commercially available in a select number of international markets. Hyperfine, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine, Inc. Forward-Looking Statements This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, expectations about the Company’s financial and operating results, including, the Company’s expected revenue and cash burn for the full year 2026, the Company's cash runway, the Company’s goals and commercial plans, including the Company’s commercial rollout of the Company’s Optive AITM software and next generation Swoop® system, the acceleration of the adoption of the Swoop® system across multiple sites of care in the hospital, neurology office and international markets, the benefits of the Company’s products and services, progress on improvements and advancements in the Company’s products and services, and the Company’s future performance, including its financial performance, and its ability to implement its strategy. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s ability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the ability of the Company to raise financing in the future; the ability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the ability of the Company to identify, in-license or acquire additional technology; the ability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the ability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; the Company’s ability to successfully complete and generate positive data from the PRIME study, ACTION PMR study, Contrast PMR study, CARE PMR study and NEURO PMR study; the Company’s ability to generate clinical evidence of the benefits of the Company’s products and services and to progress on product advancements and improvements; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based. HYPERFINE, INC. AND SUBSIDIARIES CONDENSED CONSOLIDATED BALANCE SHEETS (in thousands, except share and per share amounts) (Unaudited)       March 31,
2026     December 31,
2025   ASSETS             CURRENT ASSETS:             Cash and cash equivalents   $ 40,778     $ 35,085   Restricted cash     500       957   Accounts receivable, less allowance of $534 and $1,372 as of March 31, 2026 and December 31, 2025, respectively     3,791       5,254   Unbilled receivables     2,006       1,268   Inventories     6,327       7,090   Prepaid expenses and other current assets     2,631       1,255   Property and equipment, net     56,033       50,909   Other long term assets     2,503       2,549   Total assets     1,803       1,804   LIABILITIES AND STOCKHOLDERS’ EQUITY   $ 60,339     $ 55,262   CURRENT LIABILITIES:             Accounts payable   $ 4,552     $ 4,051   Deferred grant funding     500       957   Deferred revenue     1,578       1,544   Due to related parties     56       50   Accrued expenses and other current liabilities     3,468       5,130   Total current liabilities     10,154       11,732   Long-term debt, net     13,123       —   Warrant liabilities     1,971       1,730   Long term deferred revenue     713       729   Other noncurrent liabilities     17       66   Total liabilities     25,978       14,257                 STOCKHOLDERS' EQUITY             Class A Common stock, $0.0001 par value per share; 600,000,000 shares authorized; 83,464,909 and 82,166,458 shares issued and outstanding at March 31, 2026 and December 31, 2025, respectively     8       8   Class B Common stock, $0.0001 par value per share; 27,000,000 shares authorized; 15,055,288 shares issued and outstanding at March 31, 2026 and December 31, 2025, respectively     2       2   Additional paid-in capital     372,990       371,011   Accumulated deficit     (338,639 )     (330,016 ) Total stockholders' equity     34,361       41,005   TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY   $ 60,339     $ 55,262   HYPERFINE, INC. AND SUBSIDIARIES CONDENSED CONSOLIDATED STATEMENT OF OPERATIONS AND COMPREHENSIVE LOSS (in thousands, except share and per share amounts) (Unaudited)       Three Months Ended
March 31,       2026     2025   Sales             Device   $ 3,257     $ 1,522   Service     646       615   Total sales   $ 3,903     $ 2,137   Cost of sales             Device   $ 1,646     $ 985   Service     278       269   Total cost of sales   $ 1,924     $ 1,254   Gross profit     1,979       883   Operating Expenses:             Research and development   $ 3,845     $ 5,037   General and administrative     4,130       4,208   Sales and marketing     2,562       2,540   Total operating expenses   $ 10,537     $ 11,785   Loss from operations   $ (8,558 )   $ (10,902 ) Interest income   $ 254     $ 317   Interest expense     (83 )     —   Change in fair value of warrant liabilities     (241 )     1,618   Other income (expense), net     5       (451 ) Loss before provision for income taxes   $ (8,623 )   $ (9,418 ) Provision for income taxes     —       —   Net loss and comprehensive loss   $ (8,623 )   $ (9,418 ) Net loss per common share attributable to common stockholders, basic and diluted   $ (0.09 )   $ (0.12 ) Weighted-average shares used to compute net loss per share attributable to common stockholders, basic and diluted     97,695,133       75,697,199   HYPERFINE, INC. AND SUBSIDIARIES CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS (in thousands) (Unaudited)       Three Months Ended March 31,       2026     2025   Cash flows from operating activities:             Net loss   $ (8,623 )   $ (9,418 ) Adjustments to reconcile net loss to net cash used in operating activities:             Depreciation     274       229   Stock-based compensation expense     647       945   Loss on disposal of property and equipment, net     5       —   Change in fair value of warrant liabilities     241       (1,618 ) Amortization of debt discount and issuance costs     17       —   Other     6       11   Changes in assets and liabilities:             Accounts receivable, net     1,463       626   Unbilled receivables     (738 )     412   Inventory     763       1,193   Prepaid expenses and other current assets     (1,401 )     (1,241 ) Other long term assets     (69 )     128   Accounts payable     504       600   Deferred grant funding     (457 )     413   Deferred revenue     18       (80 ) Due to related parties     6       (7 ) Accrued expenses and other current liabilities     (1,667 )     (1,435 ) Operating lease liabilities, net     3       (7 ) Net cash used in operating activities   $ (9,008 )   $ (9,249 ) Cash flows from investing activities:             Purchases of property and equipment     (242 )     (472 ) Net cash used in investing activities   $ (242 )   $ (472 ) Cash flows from financing activities:             Proceeds from issuance of debt, net   $ 13,641     $ —   Proceeds from exercise of stock options     42       33   Proceeds from issuance of Class A common stock under “at-the-market” offering program, net     803       129   Proceeds from issuance of Class A common stock with warrants under February 2025 Offering, net     —       5,420   Net cash provided by financing activities   $ 14,486     $ 5,582   Net increase (decrease) in cash and cash equivalents and restricted cash     5,236       (4,139 ) Cash, cash equivalents and restricted cash, beginning of period     36,042       37,673   Cash, cash equivalents and restricted cash, end of period   $ 41,278     $ 33,534   Reconciliation of cash, cash equivalents, and restricted cash reported in the balance sheets             Cash and cash equivalents   $ 40,778     $ 33,093   Restricted cash     500       441   Total cash, cash equivalents and restricted cash   $ 41,278     $ 33,534   Supplemental disclosure of noncash information:             Issuance of warrants in connection with Loan Agreement, net   $ 495     $ —   Initial measurement of warrant liabilities   $ —     $ 2,858   Unpaid purchase of property and equipment   $ 28     $ 509   Unpaid debt issuance and financing costs   $ 15     $ 238     View source version on businesswire.com: https://www.businesswire.com/news/home/20260512320170/en/ Investor Contact
Webb Campbell
Gilmartin Group LLC
webb@gilmartinir.com Original: Hyperfine, Inc. Reports First Quarter 2026 Financial Results

HYPR ... the RSI remains way above 70, over 80 I believe. I took half off the table and will watch to fully reload when the chart looks more sustainable, with more clear upside. That said, I've been trading this one for so long, I'm comfortable being overweight with half the shares I had at $1.30. It could rocket up to $2.50 any time IMO.

So much upside with this business model IMO. But, watching for the RSI to hit 70 or even closer to 50. Doubt it can get to 50, much less 30 (extra strong buy zone IMO) before it rallies up to finally fill the gap at $2... and quite possibly go far higher. $2.30 would be easy on a future rally with millions of shares being accumulated.

HYPR.............................p/m

HYPR..............................https://stockcharts.com/sc3/ui/?s=HYPR&p=w&b=5&g=0&id=p86431144783

$HYPR: Thats the news it need to breakout BullFlag...............


Now $1.50

Perfect timing for that to get it boosted


GO $HYPR

Hyperfine Swoop® System Introduced as India’s First Portable MRI for Bedside Brain Imaging at the Country’s Leading Medical InstitutionApril 29, 2026 8:15 AM
Business Wire
The All India Institute of Medical Sciences, New Delhi, in partnership with Radiosurgery Global India, begins clinical use of the Hyperfine Swoop® portable MRI system


Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—and the All India Institute of Medical Sciences (AIIMS), New Delhi, India's foremost medical institution, today announced that AIIMS New Delhi has initiated clinical use of the Swoop® portable MRI system. AIIMS New Delhi is the first hospital in India to deploy bedside MRI for routine clinical use, marking an important milestone for neurological care across the country.


In a collaboration between Radiosurgery Global Ltd. (the exclusive Swoop® system distributor in India) and AIIMS New Delhi's Centre for Neurological Conditions, the Swoop® system is now performing bedside brain imaging for routine clinical care under the leadership of Dr. Shailesh Gaikwad, Head of the Department of Neuroimaging and Interventional Neuroradiology and Chief of the Neuroscience Centre at AIIMS New Delhi.


“Bedside brain imaging transforms how we care for our most critically ill patients. At AIIMS, we manage thousands of stroke and ICU patients annually, where rapid neuroimaging is essential—yet transport to conventional MRI is often unsafe or impossible. The Swoop® system eliminates that barrier. Now our clinicians can obtain diagnostic images at the point of care, enabling faster decision-making in neurology, trauma, and critical care. For a medical institution like ours that serves as a referral center across India, this deployment signals what's possible when technology and clinical need align to advance neurological care,” said Dr. Shailesh Gaikwad, Head, Department of Neuroimaging and Interventional Neuroradiology and Chief of Neuroscience Centre AIIMS New Delhi.


Why This Matters for India


India is home to over a billion people across diverse geographies, including urban megacities, remote districts, rural communities, and everything in between. Across this landscape, timely access to neuroimaging remains a significant challenge. When patients suffer a stroke, sustain a brain injury, or present with a neurological emergency, the imaging required for diagnosis and treatment is often delayed or unavailable.


Conventional high-field MRI systems require dedicated shielded rooms, specialized infrastructure, and patient transport. For critically ill patients in ICUs, trauma bays, neurosurgery wards, neonatal units, and emergency departments, transport is often not feasible. These limitations can delay diagnosis and treatment and impact outcomes.


The Swoop® system addresses these barriers by bringing MRI directly to the point of care. It requires no dedicated room, specialized power, or patient transfer. Clinicians can roll the system to the patient’s bedside in the ICU, trauma center, stroke unit, or neonatal ward and obtain brain images when and where they are needed most.


The Breadth of Clinical Impact


The Swoop® system supports a wide range of unmet clinical needs across India’s healthcare ecosystem:



Neurology and Stroke: Rapid bedside brain imaging to support timely assessment and decision-making in acute stroke care without the risks associated with patient transfer.




Emergency Care and Trauma: Timely bedside assessment of traumatic brain injury in clinical settings where speed of diagnosis is critical.




Critical Care and ICU: Ongoing neurological monitoring for critically ill patients without disrupting intensive care workflows.




Pediatric Care: Safe, accessible brain imaging for infants in PICUs, where conventional MRI is often inaccessible or clinically impractical.




Outpatient Neurology and GP Practices: Community-based point-of-care brain imaging that supports screening and streamlined referral pathways.


Neurosurgery: Post-operative monitoring without moving vulnerable patients.



Deployment at AIIMS New Delhi marks the beginning of broader adoption across India, bringing point-of-care brain imaging to clinical environments where it can have the greatest impact.


“Bringing the Swoop® system to AIIMS New Delhi is an important milestone following regulatory approval last December. India has a significant unmet need for accessible brain imaging. Deployment at the country’s leading institution signals the start of bringing point-of-care brain MRI to sites of care and institutions across India, where it can serve clinicians and their patients across neurological conditions,” said Maria Sainz, President and CEO of Hyperfine.


“Radiosurgery Global exists to democratize access to transformative technologies. We're proud that the Swoop® system's first clinical deployment in India is at AIIMS New Delhi—an institution that shares our commitment to advancing patient care across this vast, underserved landscape. This isn't just a regulatory or commercial milestone—it's the beginning of changing outcomes for critically ill patients in ICUs, trauma units, and stroke centers nationwide,” said Kapil Kalra, Managing Director, Radiosurgery Global Ltd.


A Platform for Clinical Research and Discovery


The Swoop® system deployment at AIIMS New Delhi also establishes a foundation for clinical research. As a leading center for neuroscience research and clinical innovation, AIIMS New Delhi is uniquely positioned to generate real-world evidence to guide the adoption and utilization of portable MRI across India. The AIIMS New Delhi team plans to document outcomes, contribute to peer-reviewed publications, and advance India’s role in the growing global evidence base for point-of-care brain imaging.


For more information about the Swoop® system, please visit HyperfineMRI.com.


About the Swoop® Portable MRI Systems

The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis.


About Hyperfine, Inc.

Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com.


About AIIMS New Delhi

The All India Institute of Medical Sciences (AIIMS), New Delhi, established in 1956, is India's premier autonomous public medical university and national referral center for tertiary healthcare, medical education, and biomedical research. AIIMS New Delhi consistently ranks as the number one hospital in India and trains thousands of specialists who go on to shape clinical practice nationwide. The Centre for Neurological Conditions (CNC) at AIIMS New Delhi is one of India's foremost centers for neurological care, research, and innovation.


About Radiosurgery Global Ltd.

Radiosurgery Global Ltd. (RSG), operating through its Indian entity Jona Tech Systems Pvt. Ltd., is the exclusive authorized distributor of the Hyperfine Swoop® system across India. RSG is a vertically integrated advanced medical technology company headquartered in London with offices in New Delhi, Munich, Dubai, Singapore, Jakarta, and Sydney, focused on driving innovative technologies into high-growth markets and expanding patient access to world-class diagnostics.


Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine.


Forward-Looking Statements

This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the inability to maintain the listing of the Company’s Class A common stock on the Nasdaq Stock Market; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future; the inability of the Company to progress on product advancements and improvements; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; anticipated National Institutes of Health funding pressures; the effect of U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260429706357/en/
Media

Devin Zell

Hyperfine

dzell@hyperfine.io
Investor

Webb Campbell

Gilmartin Group LLC

webb@gilmartinir.com


Original: Hyperfine Swoop® System Introduced as India’s First Portable MRI for Bedside Brain Imaging at the Country’s Leading Medical Institution

Hyperfine, Inc. to Announce First Quarter 2026 Financial Results on May 12, 2026April 28, 2026 4:05 PM
Business Wire
Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced that it will report financial results for the first quarter 2026 on Tuesday, May 12, 2026. Management will host a corresponding conference call at 1:30 p.m. Pacific Time / 4:30 p.m. Eastern Time.


A live audio webcast and an archive of the recording will be available through the Investors page of Hyperfine, Inc.’s corporate website at https://investors.hyperfine.io/. Participants are encouraged to register more than 15 minutes before the start of the call.


For more information about the Swoop® system, please visit HyperfineMRI.com.


About the Swoop® Portable MRI Systems


The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis.


About Hyperfine, Inc.


Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260428615786/en/
Media Contact

Devin Zell

Hyperfine

dzell@hyperfine.io


Investor Contact

Webb Campbell

Gilmartin Group LLC

webb@gilmartinir.com


Original: Hyperfine, Inc. to Announce First Quarter 2026 Financial Results on May 12, 2026

Hyperfine Receives CE and UKCA Marks for Next-Generation Swoop® System and Latest Advancement in Optive AI™ SoftwareApril 9, 2026 8:15 AM
Business Wire
This milestone unlocks Hyperfine’s most significant technology innovations to date for clinicians and patients across Europe and the United Kingdom, delivering a transformative leap in image quality and a major expansion of clinical capability for European markets


Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable MRI system for the brain—the Swoop® system—today announced it has received CE Marking and UK Conformity Assessment (UKCA) approval for both the next-generation Swoop® system and the latest advancement in its Optive AI™ software. Together, these regulatory approvals enable commercialization of Hyperfine’s most advanced portable MRI technology across Europe and the United Kingdom (UK), expanding access to high-quality brain imaging at the point of care and representing a pivotal milestone in the company’s international commercial growth strategy.


The next-generation Swoop® scanner, which was cleared by the FDA in the second quarter of 2025, represents a significant advancement in portable brain MRI, delivering substantial improvements in image quality, workflow, and overall user experience. The next-generation Swoop® system has generated strong customer interest in the US market, where Hyperfine has placed systems in critical care and emergency rooms of hospitals, as well as in neurology offices.


In addition, Hyperfine received European approvals for the latest advancement in its Optive AI™ software, which was cleared by the FDA in December 2025. The new software includes a new multi-direction diffusion-weighted imaging (DWI) sequence that acquires and averages images from multiple diffusion directions, similar to the method used in high-field MRI scanners. This capability produces cleaner, more consistent images that are especially valuable for stroke diagnosis, enabling better detection of small strokes and enhancing the value of the Swoop® system in acute neurological care. The software is part of the next-generation Swoop® system and is also available as a standalone software upgrade, so existing users benefit from the same powerful imaging platform.


These approvals cover markets across the European Economic Area and the United Kingdom, representing a significant global healthcare market opportunity. The Swoop® system is currently commercialized in these markets through a strong network of distributors across over a dozen countries.


“We are proud to bring our most innovative technology to clinicians and patients in Europe and the UK and are thrilled to have achieved these approvals ahead of our internal expectations,” said Maria Sainz, President and CEO of Hyperfine. “This milestone is a testament to the exceptional execution of our product and regulatory teams and meaningfully advances a key pillar of Hyperfine’s 2026 international growth strategy. We believe that the next-generation Swoop® system will accelerate international adoption of our technology and strengthen our position as the global leader in AI-powered portable brain imaging.”


Hyperfine plans to initiate commercialization of the next-generation Swoop® system and the latest Optive AI™ software in Europe and the UK early in the third quarter of 2026.


For more information about the Swoop® system, please visit HyperfineMRI.com.


About the Swoop® Portable MRI Systems


The Swoop® Portable MR Imaging® Systems are U.S. Food and Drug Administration (FDA) cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis.


About Hyperfine, Inc.


Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit HyperfineMRI.com.


Hyperfine, the Hyperfine logo, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine. The Swoop logo, Optive AI logo, and Optive AI are trademarks of Hyperfine.


Forward-Looking Statements


This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, the Company’s goals and commercial plans, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy, including its entrance into new markets. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the inability to maintain the listing of the Company’s Class A common stock on the Nasdaq Stock Market; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future; the inability of the Company to progress on product advancements and improvements; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; anticipated National Institutes of Health funding pressures; the effect of U.S. export controls and tariffs; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements, which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260409030745/en/
Media Contact

Devin Zell

Hyperfine

dzell@hyperfine.io


Investor Contact

Webb Campbell

Gilmartin Group LLC

webb@gilmartinir.com


Original: Hyperfine Receives CE and UKCA Marks for Next-Generation Swoop® System and Latest Advancement in Optive AI™ Software

Thanks for this, first I've seen it. Overweight on HYPR ... sure looks ready to break out to me. CEO incentives look strong now too. New filing this past Thurs eve..

How Decentralized AI is Unlocking Value in Cardiac DiagnosticsMarch 27, 2026 9:30 AM
PR Newswire (US)

ISSUED ON BEHALF OF VENTRIPOINT DIAGNOSTICS LTD.VANCOUVER,BC, March 27, 2026 /PRNewswire/ -- USANewsGroup.com News Commentary – Heart disease is a quiet crisis that is draining healthcare resources worldwide, currently costing the European Union over €282 billion annually while tragically claiming 1.7 million lives a year[1]. This immense structural pressure is acting as a catalyst for smart money, with institutional capital rapidly accumulating positions in scalable, AI-enabled diagnostic platforms. In fact, peer-reviewed data now confirms that AI-driven healthcare startups command the largest share of venture funding in the entire biopharmaceutical sector[2]. At the center of this pivotal transition are five companies building the infrastructure for the next cycle of predictive cardiology: VentriPoint Diagnostics (TSXV: VPT) (OTCPK: VPTDF), HeartBeam (NASDAQ: BEAT), Heartflow (NASDAQ: HTFL), Hyperfine (NASDAQ: HYPR), and GE Healthcare Technologies (NASDAQ: GEHC).







This momentum is not just financial; it is heavily backed by the highest levels of medical regulation. The FDA's authorized registry of AI medical devices has just surpassed 1,200 approved products, with cardiovascular applications emerging as the second largest category overall[3]. This robust regulatory tailwind perfectly aligns with a severe clinical urgency. According to the landmark JACC Cardiovascular Statistics 2026 report, nearly half of all American adults now meet the criteria for hypertension. Because broader treatment and control rates have remained stagnant for over a decade, the market is making it clear that scalable, decentralized AI imaging solutions are the ultimate value drivers for this next healthcare cycle[4].VentriPoint Diagnostics (TSXV: VPT) (OTCPK: VPTDF) is expanding into remote healthcare after announcing a partnership with First Light Health, an Indigenous-owned medical services company based in Vancouver, to deliver AI-powered cardiac diagnostics to Indigenous and remote communities across Canada.Together, the two companies are developing a hub-and-spoke care model built around VentriPoint's VMS+™ system. Local providers in remote areas will capture ultrasound scans on-site and be supported by specialists at a central hub who are able to digitally access images and assist with interpretation. That gives patients in British Columbia, Yukon, Alberta, Manitoba, and New Brunswick access to advanced cardiac imaging without travelling hundreds of kilometres, at lower cost and with faster turnaround than traditional referral pathways. Following validation of the model, Ventripoint plans to scale it beyond Canada into underserved communities globally.VentriPoint's VMS+™ system converts standard 2D echocardiograms into detailed 3D volumetric images. The company says its accuracy is comparable to cardiac MRI, but at a fraction of the cost and without the infrastructure those machines require. For communities where heart disease rates are high and specialist access is limited, the difference between early diagnosis and late diagnosis can be the difference between treatment and tragedy."Cardiovascular disease doesn't respect geography, but too often, access to cardiac care does," said Hugh MacNaught, CEO of VentriPoint Diagnostics. "Our work with First Light Health and other First Nations partners such as the Nisga_'a Valley Health Authority demonstrates the need for a made-in-Canada innovation that can close that gap. We see the potential for this solution to be widely deployed, from the Arctic to the Amazon. This is what scalable, equitable heart care looks like."First Light Health brings cultural safety expertise and established relationships within First Nations communities, which matters when deploying health technology in populations that have historically been underserved by the broader system.The partnership builds on recent commercial traction. VentriPoint signed a commercial agreement with LG Consulting Solutions to support VMS+™ deployment across Northern California, targeting cardiac centres in the Sacramento and San Francisco regions. Before that, the company had already partnered with the Nisga_'a Valley Health Authority to pilot a similar model in northern BC.VentriPoint is a Toronto-based medtech company with regulatory approvals in the United States, Canada, and Europe. Its VMS+™ platform works with ultrasound equipment from any vendor and is built on over a decade of Knowledge Based Reconstruction technology development. The goal is simple: put MRI-grade cardiac diagnostics within reach of any clinic or community that needs them.CONTINUED… Read this and more news for VentriPoint Diagnostics at:  https://usanewsgroup.com/2025/11/21/the-mri-grade-disruption-hiding-in-plain-sight-why-the-smart-money-is-watching-ventripointIn other industry developments and happenings in the market include:HeartBeam (NASDAQ: BEAT) recently announced a strategic AI collaboration with the Icahn School of Medicine at Mount Sinai to jointly develop and validate next-generation AI-ECG algorithms using HeartBeam's patented 3D ECG platform, which is the only system capable of collecting synthesized 12-lead ECG data from patients in the home setting continuously over time. The partnership combines HeartBeam's longitudinal real-world ECG datasets with Mount Sinai's clinically annotated 12-lead data to accelerate training of personalized cardiac AI models for applications including heart attack risk assessment."We believe expanding access to 12-lead ECG data assessment beyond the clinic is one of the biggest opportunities," said Robert Eno, CEO of HeartBeam. "By pairing our ability to gather high-fidelity real-world ECG data with Mount Sinai's extensive clinical data resources and AI expertise, we are creating a differentiated cardiac intelligence engine that can scale beyond traditional care settings and broaden the reach of predictive cardiology, ultimately expanding our clinical and commercial opportunity."HeartBeam's 3D ECG technology received FDA clearance for arrhythmia assessment in December 2024 and for 12-lead ECG synthesis in December 2025, providing a regulatory foundation for the expanded AI applications this collaboration targets. The resulting data engine is expected to support entry into new clinical indications and reimbursement pathways over time.Heartflow (NASDAQ: HTFL) announced new clinical evidence and a landmark registry launch at the American College of Cardiology Annual Scientific Session, with data from a 15,000-patient registry showing that high plaque volume independently predicts a fourfold increase in major adverse cardiovascular events regardless of conventional risk factors or stenosis severity. Simultaneously, Heartflow enrolled the first patient in the NAVIGATE-PCI Registry, a 5,000-patient study assessing the real-world impact of AI-guided CT-based pre-procedural planning on clinical strategy and physician confidence in the catheterization lab."These milestones reflect tremendous progress toward Heartflow's goal of transforming coronary artery disease from the world's leading cause of death into a condition that can be detected early, diagnosed accurately, and managed for life," said Campbell Rogers, M.D., F.A.C.C., Chief Medical Officer at Heartflow. "The Heartflow Plaque Analysis data presented at ACC and the launch of the NAVIGATE-PCI Registry represent important steps in building the rigorous real-world evidence needed to support AI-driven decision-making across the full continuum of cardiovascular care."Heartflow has now been adopted by more than 1,400 institutions globally and its technology is backed by over 600 peer-reviewed publications covering more than 500,000 patients. Commercial availability of the Heartflow PCI Navigator is expected in Q2 2026, positioning the company to expand its platform from risk stratification into guided intervention planning.Hyperfine (NASDAQ: HYPR) published breakthrough stroke detection data for its Swoop portable MRI system in the journal Stroke: Vascular and Interventional Neurology, with the next-generation scanner's advanced multi-directional DWI sequence achieving 100% sensitivity and 100% specificity for clinically relevant lesions greater than 1.0 mL, detecting strokes as small as 2.8 mm while cutting scan time by approximately 30%. The prospective multi-center study across Massachusetts General Hospital, Buffalo General Medical Center, and Yale New Haven Hospital represents the largest dataset to date evaluating portable MRI for stroke detection."Stroke detection represents a critical driver of the Swoop system's expansion into emergency departments," said Maria Sainz, President and CEO of Hyperfine. "The results from our next-generation Swoop system, combined with our new, advanced multi-direction DWI sequence that was recently cleared by the FDA, are truly remarkable. This data gives us even greater confidence that the Swoop system can reliably detect clinically relevant strokes, streamline workflows, and further strengthen the value of integrating portable MRI into stroke diagnosis and care."With FDA clearance for its multi-directional DWI sequence now secured and real-world performance validated across multiple clinical sites, Hyperfine is positioned to accelerate emergency department adoption of the Swoop platform. The system's portability and speed open new access pathways for stroke diagnosis in settings where conventional MRI is not clinically practical.GE Healthcare Technologies (NASDAQ: GEHC) announced its lead industrial role in COMPASS, a five-year, €50.5 million consortium backed by the European Union's Innovative Health Initiative and more than sixty partners focused on advancing early detection of cardiovascular toxicity in cancer patients across Europe. The program will leverage AI, advanced imaging, novel biomarkers, and integrated care pathways to address cardiotoxicity, which accounts for up to 10% of mortality in cancer survivors."This initiative is well positioned to enable patient-centered cancer care that takes cardiotoxicity risk into account, supports the early detection of cardiotoxic side-effects, and promotes long-term heart health for oncology patients," said Eigil Samset, General Manager, Cardiology Solutions at GE Healthcare and COMPASS Industry Lead. "By developing an AI-powered, integrated care pathway that connects oncologists and cardiologists in clinical practice, this collaboration has the potential to further improve cancer survival by tackling cardiovascular-related morbidity."The COMPASS grant agreement was signed on March 25, 2026 and runs for five years, with GE Healthcare positioned to advance its AI and imaging capabilities within the largest public-private healthcare partnership under the IHI framework. The initiative supports GE Healthcare's broader cardiology solutions strategy as part of its $20.6 billion global healthcare platform.Further Reading: https://usanewsgroup.com/2025/11/21/the-mri-grade-disruption-hiding-in-plain-sight-why-the-smart-money-is-watching-ventripointCONTACT:USA NEWS GROUPinfo @acblanke1DISCLAIMER: Nothing in this publication should be considered as personalized financial advice. We are not licensed under securities laws to address your particular financial situation. No communication by our employees to you should be deemed as personalized financial advice. Please consult a licensed financial advisor before making any investment decision. This is a paid advertisement and is neither an offer nor recommendation to buy or sell any security. We hold no investment licenses and are thus neither licensed nor qualified to provide investment advice. The content in this report or email is not provided to any individual with a view toward their individual circumstances. USA News Group is a wholly-owned subsidiary of Market IQ Media Group, Inc. (MIQ). This article is being distributed for Baystreet.ca media Corp, who has been paid a fee for an advertising campaign. MIQ has not been paid a fee for Ventripoint Diagnostics Ltd. advertising or digital media, but the owner/operators of MIQ also co-owns Baystreet.ca Media Corp. (BAY) There may also be 3rd parties who may have shares of Ventripoint Diagnostics Ltd. and may liquidate their shares which could have a negative effect on the price of the stock. This compensation constitutes a conflict of interest as to our ability to remain objective in our communication regarding the profiled company. Because of this conflict, individuals are strongly encouraged to not use this publication as the basis for any investment decision. The owner/operator of MIQ/BAY own shares of Ventripoint Diagnostics Ltd and reserve the right to buy and sell, and will buy and sell shares of Ventripoint Diagnostics Ltd. at any time without any further notice commencing immediately and ongoing. We also expect further compensation as an ongoing digital media effort to increase visibility for the company, no further notice will be given, but let this disclaimer serve as notice that all material, including this article, which is disseminated by MIQ on behalf of BAY has been approved by Ventripoint Diagnostics Ltd.; this is a paid advertisement, we currently own shares of Ventripoint Diagnostics Ltd. and will buy and sell shares of the company in the open market, or through private placements, and/or other investment vehicles. While all information is believed to be reliable, it is not guaranteed by us to be accurate. Individuals should assume that all information contained in our newsletter is not trustworthy unless verified by their own independent research. Also, because events and circumstances frequently do not occur as expected, there will likely be differences between the any predictions and actual results. Always consult a licensed investment professional before making any investment decision. Be extremely careful, investing in securities carries a high degree of risk; you may likely lose some or all of the investment.SOURCES:https://www.oecd.org/en/publications/the-state-of-cardiovascular-health-in-the-european-union_ea7a15f4-en/full-report/the-burden-of-cardiovascular-disease_e28210c3.html
 https://www.jmir.org/2026/1/e84968
 https://www.fda.gov/medical-devices/software-medical-device-samd/artificial-intelligence-enabled-medical-devices
 https://www.jacc.org/doi/10.1016/j.jacc.2025.12.027Logo - https://mma.prnewswire.com/media/2838876/5886720/USA_News_Group_Logo.jpg



View original content to download multimedia:https://www.prnewswire.com/news-releases/how-decentralized-ai-is-unlocking-value-in-cardiac-diagnostics-302726891.html

Original: How Decentralized AI is Unlocking Value in Cardiac Diagnostics

HYPR...............................https://stockcharts.com/sc3/ui/?s=HYPR&p=w&b=5&g=0&id=p86431144783

hypr.................................https://stockcharts.com/sc3/ui/?s=HYPR&p=W&b=5&g=0&id=p86431144783

Hyperfine, Inc. Reports Fourth Quarter and Full Year 2025 Financial ResultsMarch 18, 2026 4:05 PM
Business Wire
Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first FDA-cleared AI-powered portable magnetic resonance (MR) brain imaging system—the Swoop® system—today announced fourth quarter and full year 2025 financial results and provided a business update.


“The launch of our second-generation Swoop® scanner, our Optive AI™ software, and the addition of a new market in the neurology office setting in mid-2025 marks a new era in the adoption of portable brain MRI and the future of our company. We hold a highly proprietary and differentiated technology leadership position in the ability to produce diagnostic quality images with an ultra-low-field magnet,” said Maria Sainz, Chief Executive Officer and President of Hyperfine, Inc. “As we move through 2026, we expect to continue to see growth catalysts accelerate the adoption of the Swoop® system across multiple sites of care in the hospital, neurology office and international markets.”


Recent Achievements and Business Highlights



Obtained FDA clearance of the first Optive AI™ software update with advanced diffusion imaging capability, focused on enhancing stroke detection.



Enrolled first patient in Contrast PMR, a study designed to support a future FDA 510(k) submission to expand the Swoop® system’s intended use to include gadolinium-based contrast agents.



Presented NEURO-PMR results at the 2026 American Society of Neuroimaging showing high diagnostic value and superior patient experience in neurology clinics.



Published paper in Stroke: Vascular and Interventional Neurology (SVIN) demonstrating the Swoop® system’s enhanced stroke detection capabilities.



Published paper in Clinical Neuroimaging demonstrating the significant health economic benefit of using the Swoop® system.



Received regulatory approval in India from the Central Drugs Standard Control Organization for the first-generation Swoop® system.



Awarded $3.7 million grant from the Gates Foundation to advance global brain health.



Raised over $20 million in gross proceeds through an equity public offering in October 2025.



Secured a $40 million senior secured term loan facility in March 2026, with initial funding of $15 million and an additional $25 million available upon achievement of certain commercial milestones.



Bolstered balance sheet with expected cash runway into 2028, including recent equity financing and the initial debt tranche, providing capital for commercial growth.



Fourth Quarter 2025 Financial Results



Revenues for the fourth quarter of 2025 were $5.29 million, increasing 128% compared to $2.32 million in the fourth quarter of 2024.



Sold net 16 commercial Swoop® systems in the fourth quarter of 2025, compared to nine in the fourth quarter of 2024.



Gross profit for the fourth quarter of 2025 was $2.69 million, compared to $0.83 million in the fourth quarter of 2024, representing 51% gross margin in the fourth quarter of 2025, compared to 36% gross margin in the fourth quarter of 2024.



Research and development expenses for the fourth quarter of 2025 were $3.82 million, compared to $5.11 million in the fourth quarter of 2024.



Sales, marketing, general, and administrative expenses for the fourth quarter of 2025 were $6.54 million, compared to $6.49 million in the fourth quarter of 2024.



Net loss for the fourth quarter of 2025 was $5.91 million, equating to a net loss of $0.06 per share, as compared to a net loss of $10.39 million, or a net loss of $0.14 per share, for the fourth quarter of 2024. The fourth quarter of 2025 net loss includes a gain from the change in fair value of warrant liabilities of $1.46 million.



Full Year 2025 Financial Results



Revenues for the full year 2025 were $13.56 million, increasing 5.2% compared to $12.89 million in 2024.



Sold net 38 commercial Swoop® systems in 2025, compared to 48 in 2024.



Gross profit for the full year 2025 was $6.75 million, compared to $5.89 million in 2024, representing 50% gross margin in 2025, compared to 46% gross margin in 2024.



Research and development expenses for the full year 2025 were $17.45 million, compared to $22.50 million in 2024.



Sales, marketing, general, and administrative expenses for the full year 2025 were $26.39 million, compared to $26.62 million in 2024.



Net loss for the full year 2025 was $35.57 million, equating to a net loss of $0.43 per share, as compared to a net loss of $40.72 million, or a net loss of $0.56 per share, for 2024. The full year 2025 net loss includes a gain from the change in fair value of warrant liabilities of $0.83 million.



Cash and cash equivalents totaled $35.09 million as of December 31, 2025.



2026 Financial Guidance



Management expects revenue for the full year 2026 to be approximately $20 to $22 million, representing 55% growth at the midpoint as compared to full year 2025.



Management expects cash burn1 for the full year 2026 to be approximately $26 to $28 million, representing a 10% decline at the midpoint as compared to full year 2025.



1Cash burn is calculated as change in cash and cash equivalents less net financing proceeds.


Conference Call


Hyperfine, Inc. will host a conference call at 1:30 p.m. PT/ 4:30 p.m. ET on Wednesday, March 18, 2026 to discuss its fourth quarter and full year 2025 financial results and provide a business update. Those interested in listening should register online by visiting https://investors.hyperfine.io/ and clicking on News & Events. Participants are encouraged to register more than 15 minutes before the start of the call. A live and archived audio webcast will be available through the Investors page of Hyperfine, Inc.’s corporate website at https://investors.hyperfine.io/.


About Hyperfine, Inc. and the Swoop® Portable MR Imaging® Systems


Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first U.S. Food and Drug Administration (FDA)-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of professional care. The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. For more information, visit hyperfine.io.


The Swoop® Portable MR Imaging® systems are FDA cleared for brain imaging of patients of all ages. They are portable, ultra-low-field magnetic resonance imaging devices for producing images that display the internal structure of the head where full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. The Swoop® system also has CE Mark in the European Union and UKCA Mark in the United Kingdom. The Swoop® system is commercially available in a select number of international markets.


Hyperfine, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine, Inc.


Forward-Looking Statements


This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the “Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, expectations about the Company’s financial and operating results, including, the Company’s expected revenue and cash burn for the full year 2026, the Company's cash runway, the Company’s goals and commercial plans, including the Company’s commercial rollout of the Company’s Optive AI™ software and next generation Swoop® system, the acceleration of the adoption of the Swoop® system across multiple sites of care in the hospital, neurology office and international markets, the benefits of the Company’s products and services, progress on improvements and advancements in the Company’s products and services, and the Company’s future performance, including its financial performance, and its ability to implement its strategy. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the Company’s ability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the ability of the Company to raise financing in the future; the ability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the ability of the Company to identify, in-license or acquire additional technology; the ability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; existing and potential future National Institutes of Health funding pressures; existing and potential future effects from U.S. export controls and tariffs; the ability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; the Company’s ability to successfully complete and generate positive data from the PRIME study, ACTION PMR study, Contrast PMR study, CARE PMR study and NEURO PMR study; the Company’s ability to generate clinical evidence of the benefits of the Company’s products and services and to progress on product advancements and improvements; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in the Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based.




HYPERFINE, INC. AND SUBSIDIARIES








CONSOLIDATED BALANCE SHEETS








(in thousands, except share and per share amounts)








(Unaudited)








 






 






December 31,






 








 






 






2025






 






 






2024






 








ASSETS






 






 






 






 






 






 








CURRENT ASSETS:






 






 






 






 






 






 








Cash and cash equivalents






 






$






35,085






 






 






$






37,645






 








Restricted cash






 






 






957






 






 






 






28






 








Accounts receivable, less allowance of $1,372 and $651 in 2025 and 2024, respectively






 






 






5,254






 






 






 






5,956






 








Unbilled receivables






 






 






1,268






 






 






 






2,349






 








Inventory






 






 






7,090






 






 






 






5,832






 








Prepaid expenses and other current assets






 






 






1,255






 






 






 






1,900






 








Total current assets






 






$






50,909






 






 






$






53,710






 








Property and equipment, net






 






 






2,549






 






 






 






3,122






 








Other long term assets






 






 






1,804






 






 






 






2,069






 








Total assets






 






$






55,262






 






 






$






58,901






 








LIABILITIES AND STOCKHOLDERS' EQUITY






 






 






 






 






 






 








CURRENT LIABILITIES:






 






 






 






 






 






 








Accounts payable






 






$






4,051






 






 






$






1,607






 








Deferred grant funding






 






 






957






 






 






 






28






 








Deferred revenue






 






 






1,544






 






 






 






1,460






 








Due to related parties






 






 






50






 






 






 






61






 








Accrued expenses and other current liabilities






 






 






5,130






 






 






 






5,573






 








Total current liabilities






 






$






11,732






 






 






$






8,729






 








Warrant liabilities






 






 






1,730






 






 






 






—






 








Long term deferred revenue






 






 






729






 






 






 






1,054






 








Other noncurrent liabilities






 






 






66






 






 






 






78






 








Total liabilities






 






$






14,257






 






 






$






9,861






 








 






 






 






 






 






 






 








STOCKHOLDERS' EQUITY:






 






 






 






 






 






 








Class A Common stock, $.0001 par value; 600,000,000 shares authorized; 82,166,458 and 58,076,261 shares issued and outstanding at December 31, 2025 and 2024, respectively






 






 






8






 






 






 






5






 








Class B Common stock, $.0001 par value; 27,000,000 shares authorized; 15,055,288 shares issued and outstanding at December 31, 2025 and 2024






 






 






2






 






 






 






2






 








Additional paid-in capital






 






 






371,011






 






 






 






343,475






 








Accumulated deficit






 






 






(330,016






)






 






 






(294,442






)








Total stockholders' equity






 






$






41,005






 






 






$






49,040






 








TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY






 






$






55,262






 






 






$






58,901






 









HYPERFINE, INC. AND SUBSIDIARIES








CONSOLIDATED STATEMENT OF OPERATIONS AND COMPREHENSIVE LOSS








(in thousands, except share and per share amounts)








(Unaudited)








 






 






Three Months Ended

December 31,






 






 






Twelve Months Ended

December 31,






 








 






 






2025






 






 






2024






 






 






2025






 






 






2024






 








Sales






 






 






 






 






 






 






 






 






 






 






 






 








Device






 






$






4,857






 






 






$






1,743






 






 






$






11,398






 






 






$






10,450






 








Service






 






 






436






 






 






 






578






 






 






 






2,165






 






 






 






2,440






 








Total sales






 






$






5,293






 






 






$






2,321






 






 






$






13,563






 






 






$






12,890






 








Cost of sales






 






 






 






 






 






 






 






 






 






 






 






 








Device






 






$






2,345






 






 






$






1,107






 






 






$






5,755






 






 






$






5,387






 








Service






 






 






254






 






 






 






388






 






 






 






1,055






 






 






 






1,612






 








Total cost of sales






 






$






2,599






 






 






$






1,495






 






 






$






6,810






 






 






$






6,999






 








Gross profit






 






 






2,694






 






 






 






826






 






 






 






6,753






 






 






 






5,891






 








Operating Expenses:






 






 






 






 






 






 






 






 






 






 






 






 








Research and development






 






$






3,825






 






 






$






5,105






 






 






$






17,451






 






 






$






22,499






 








General and administrative






 






 






4,034






 






 






 






4,133






 






 






 






16,253






 






 






 






17,494






 








Sales and marketing






 






 






2,503






 






 






 






2,353






 






 






 






10,134






 






 






 






9,122






 








Total operating expenses






 






$






10,362






 






 






$






11,591






 






 






$






43,838






 






 






$






49,115






 








Loss from operations






 






$






(7,668






)






 






$






(10,765






)






 






$






(37,085






)






 






$






(43,224






)








Interest income






 






$






280






 






 






$






436






 






 






$






1,023






 






 






$






2,492






 








Change in fair value of warrant liabilities






 






 






1,464






 






 






 






—






 






 






 






825






 






 






 






—






 








Other income (expense), net






 






 






12






 






 






 






(61






)






 






 






(337






)






 






 






12






 








Loss before provision for income taxes






 






$






(5,912






)






 






$






(10,390






)






 






$






(35,574






)






 






$






(40,720






)








Provision for income taxes






 






 






—






 






 






 






—






 






 






 






—






 






 






 






—






 








Net loss and comprehensive loss






 






$






(5,912






)






 






$






(10,390






)






 






$






(35,574






)






 






$






(40,720






)








Net loss per common share attributable to common stockholders, basic and diluted






 






$






(0.06






)






 






$






(0.14






)






 






$






(0.43






)






 






$






(0.56






)








Weighted-average shares used to compute net loss per share attributable to common stockholders, basic and diluted






 






 






94,204,138






 






 






 






72,990,908






 






 






 






81,795,105






 






 






 






72,413,541






 









HYPERFINE, INC. AND SUBSIDIARIES








CONSOLIDATED STATEMENT OF CASH FLOWS








(in thousands)








(Unaudited)








 






 






Year Ended December 31,






 








 






 






2025






 






 






2024






 








Cash flows from operating activities:






 






 






 






 






 






 








Net loss






 






$






(35,574






)






 






$






(40,720






)








Adjustments to reconcile net loss to net cash used in operating activities:






 






 






 






 






 






 








Depreciation






 






 






1,090






 






 






 






1,009






 








Stock-based compensation expense






 






 






2,801






 






 






 






4,362






 








Write-off of equipment






 






 






121






 






 






 






215






 








Change in fair value of warrant liabilities






 






 






(825






)






 






 






—






 








Other






 






 






27






 






 






 






(11






)








Changes in assets and liabilities






 






 






 






 






 






 








Accounts receivable






 






 






702






 






 






 






(2,767






)








Unbilled receivables






 






 






1,081






 






 






 






(1,407






)








Inventory






 






 






(1,475






)






 






 






562






 








Prepaid expenses and other current assets






 






 






436






 






 






 






(222






)








Prepaid inventory






 






 






—






 






 






 






693






 








Other long term assets






 






 






240






 






 






 






325






 








Accounts payable






 






 






2,427






 






 






 






382






 








Deferred grant funding






 






 






929






 






 






 






(593






)








Deferred revenue






 






 






(241






)






 






 






93






 








Due to related parties






 






 






(11






)






 






 






—






 








Accrued expenses and other current liabilities






 






 






332






 






 






 






(683






)








Operating lease liabilities, net






 






 






(8






)






 






 






(5






)








Net cash used in operating activities






 






$






(27,948






)






 






$






(38,767






)








Cash flows from investing activities:






 






 






 






 






 






 








Purchases of property and equipment






 






 






(1,185






)






 






 






(383






)








Net cash used in investing activities






 






$






(1,185






)






 






$






(383






)








Cash flows from financing activities:






 






 






 






 






 






 








Proceeds from exercise of stock options






 






$






156






 






 






$






171






 








Proceeds from issuance of Class A common stock under “at-the-market” offering program, net






 






 






3,383






 






 






 






848






 








Proceeds from issuance of Class A common stock with warrants under February 2025 Offering, net






 






 






5,183






 






 






 






—






 








Proceeds from issuance of Class A common stock under October 2025 Offering, net






 






 






18,443






 






 






 






—






 








Proceeds from issuance of Class A common stock in connection with warrant exercises






 






 






337






 






 






 






—






 








Net cash provided by financing activities






 






$






27,502






 






 






$






1,019






 








Net decrease in cash and cash equivalents and restricted cash






 






 






(1,631






)






 






 






(38,131






)








Cash, cash equivalents and restricted cash, beginning of year






 






 






37,673






 






 






 






75,804






 








Cash, cash equivalents and restricted cash, end of year






 






$






36,042






 






 






$






37,673






 








Reconciliation of cash, cash equivalents, and restricted cash reported in the balance sheets






 






 






 






 






 






 








Cash and cash equivalents






 






$






35,085






 






 






$






37,645






 








Restricted cash






 






 






957






 






 






 






28






 








Total cash, cash equivalents and restricted cash






 






$






36,042






 






 






$






37,673






 








Supplemental disclosure of noncash information:






 






 






 






 






 






 








Noncash acquisition of property and equipment






 






$






217






 






 






$






765






 








Unpaid purchase of property and equipment






 






$






31






 






 






$






—






 








Initial measurement of warrant liabilities






 






$






2,858






 






 






$






—






 







 

View source version on businesswire.com: https://www.businesswire.com/news/home/20260318436530/en/
Investor Contact

Webb Campbell

Gilmartin Group LLC

webb@gilmartinir.com


Original: Hyperfine, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results