NanoVibronix Advances Development of PainShield and UroShield with Completion of NextGen Prototypes
2025年1月7日 - 10:00PM
ビジネスワイヤ(英語)
Development advancing to verification and
testing phase; Aims to future-proof design, lower componentry costs
and improve manufacturing
NanoVibronix, Inc. (NASDAQ: NAOV) (the “Company”),
a medical device company that produces the UroShield®, PainShield®
and WoundShield® Surface Acoustic Wave (SAW) Portable Ultrasonic
Therapeutic Devices, today announced a third-party contractor
engaged by the Company has completed the design phase for the
development of the Company’s next generation PainShield® and
UroShield® devices.
During the design phase, which was completed in December 2024,
the third-party contractor developed prototypes of the Company’s
next generation PainShield® and UroShield® devices that aim to
reduce both the cost of assembly and the risk profile and minimize
user burden.
Brian Murphy, Chief Executive Officer of the Company, commented,
“We are pleased with the work the development team completed during
the design phase. The prototypes were delivered on-time and within
budget, and we are now eager to move forward to the next phase for
further validation and testing. We are continuously seeking
opportunities to advance our products, drive operational
improvements in our business and evolve our products for the
benefit of the patients who use them. Completion of this phase
represents a major milestone towards our ultimate goal of broader
adoption by the healthcare community of PainShield and UroShield
and increasing unit sales.”
Design Updates Include:
- Additional mode of therapy to enhance the user
experience and improve efficacy.
- Future-Proofing and Optimization of Componentry: The
design has been updated to ensure that its current components will
remain readily available throughout the manufacturing and
commercialization process.
- Streamlining the Software: Efforts have been made to
simplify and optimize the software for better performance and ease
of use.
- Enhancements to the User Interface: The actuator cable
has been redesigned to feature USB-C connectors, and a single lead
will now be used for the UroShield® model, enhancing user
experience and simplifying device setup.
- Improvements to design to promote cost effective
production and regulatory compliance.
The Company is moving to the next phase of development, which
will involve further validation and testing based on feedback and
protocols the Company has received to date.
About NanoVibronix, Inc.
NanoVibronix, Inc. (NASDAQ: NAOV) is a medical device company
headquartered in Tyler, Texas, with research and development in
Nesher, Israel, focused on developing medical devices utilizing its
patented low intensity surface acoustic wave (SAW) technology. The
proprietary technology allows for the creation of low-frequency
ultrasound waves that can be utilized for a variety of medical
applications, including for disruption of biofilms and bacterial
colonization, as well as for pain relief. The devices can be
administered at home without the continuous assistance of medical
professionals. The Company’s primary products include PainShield®
and UroShield®, which are portable devices suitable for
administration at home or in any care setting. Additional
information about NanoVibronix is available at:
www.nanovibronix.com.
Forward-looking Statements
This press release contains “forward-looking statements.” Such
statements may be preceded by the words “intends,” “may,” “will,”
“plans,” “expects,” “anticipates,” “projects,” “predicts,”
“estimates,” “aims,” “believes,” “hopes,” “potential” or similar
words. Forward-looking statements are not guarantees of future
performance, are based on certain assumptions and are subject to
various known and unknown risks and uncertainties, many of which
are beyond the Company’s control, and cannot be predicted or
quantified; consequently, actual results may differ materially from
those expressed or implied by such forward-looking statements. Such
risks and uncertainties include, without limitation, risks and
uncertainties associated with: (i) market acceptance of our
existing and new products or lengthy product delays in key markets;
(ii) negative or unreliable clinical trial results; (iii) inability
to secure regulatory approvals for the sale of our products; (iv)
intense competition in the medical device industry from much
larger, multinational companies; (v) product liability claims; (vi)
product malfunctions; (vii) our limited manufacturing capabilities
and reliance on subcontractor assistance; (viii) insufficient or
inadequate reimbursements by governmental and/or other third party
payers for our products; (ix) our ability to successfully obtain
and maintain intellectual property protection covering our
products; (x) legislative or regulatory reform impacting the
healthcare system in the U.S. or in foreign jurisdictions; (xi) our
reliance on single suppliers for certain product components, (xii)
the need to raise additional capital to meet our future business
requirements and obligations, given the fact that such capital may
not be available, or may be costly, dilutive or difficult to
obtain; (xiii) our conducting business in foreign jurisdictions
exposing us to additional challenges, such as foreign currency
exchange rate fluctuations, logistical and communications
challenges, the burden and cost of compliance with foreign laws,
and political and/or economic instabilities in specific
jurisdictions; and (xiv) market and other conditions. More detailed
information about the Company and the risk factors that may affect
the realization of forward-looking statements is set forth in the
Company’s filings with the Securities and Exchange Commission
(“SEC”), including the Company’s Annual Report on Form 10-K and its
Quarterly Reports on Form 10-Q. Investors and security holders are
urged to read these documents free of charge on the SEC’s web site
at: http://www.sec.gov. The Company assumes no obligation to
publicly update or revise its forward-looking statements as a
result of new information, future events, or otherwise, except as
required by law.
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version on businesswire.com: https://www.businesswire.com/news/home/20250107583432/en/
Investor Contact:
Brett Maas, Managing Principal, Hayden IR, LLC
brett@haydenir.com (646) 536-7331
NanoVibronix (NASDAQ:NAOV)
過去 株価チャート
から 12 2024 まで 1 2025
NanoVibronix (NASDAQ:NAOV)
過去 株価チャート
から 1 2024 まで 1 2025