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NanoVibronix Regains Nasdaq Compliance ELMSFORD, N.Y.

Key Takeaway: NanoVibronix, Inc. has confirmed its compliance with Nasdaq's listing requirements as of November 20, 2023, ensuring the company's continued presence on The Nasdaq Capital Market. This follows the company's fulfillment of the minimum stockholders' equity requirement of $2.5 million. The matter of listing previously disclosed to the public has now been officially closed, marking a positive development for the company and its shareholders.

Market Sentiment Analysis

POSITIVE FACTORS

  • NanoVibronix has regained compliance with Nasdaq listing requirements.
  • The company has demonstrated sufficient stockholders' equity.
  • The closure of the listing matter signifies stability for shareholders.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Cash runway
~0 mo
High dilution risk
Lead asset
NG Shield
Phase 2 · Intubation, Nasogastric

Full Press Release Details

Regains Nasdaq Compliance
N.Y., Nov. 21, 2023 (Business Wire) -- NanoVibronix, Inc., (NASDAQ: NAOV) (the "Company"), a medical device
company that produces the UroShield and PainShield Surface Acoustic Wave (SAW) Portable Ultrasonic Therapeutic Devices, today
announced that on November 20, 2023, the Company received official notice from The Nasdaq Stock Market LLC that the Company has evidenced
compliance with all applicable criteria for continued listing on The Nasdaq Capital Market, including the minimum stockholders'
equity requirement of $2.5 million. Accordingly, the previously disclosed listing matter has been closed.
Inc. (NASDAQ: NAOV) is a medical device company headquartered in Elmsford, New York, 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 assistance of
medical professionals. The Company's primary products include PainShield , UroShield and WoundShield , all of which
are portable devices suitable for administration at home without assistance of medical professionals. Additional information about NanoVibronix
is available at: www.nanovibronix.com.
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, e.g., 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.
Maas, Managing Principal, Hayden IR, LLC

Frequently Asked Questions

What compliance notice did NanoVibronix receive?

On November 20, 2023, NanoVibronix received notice of compliance with Nasdaq criteria.

What are the primary products of NanoVibronix?

NanoVibronix's main products are PainShield, UroShield, and WoundShield.

Where is NanoVibronix headquartered?

NanoVibronix is headquartered in Elmsford, New York.

What technology does NanoVibronix use in its devices?

NanoVibronix utilizes patented low intensity surface acoustic wave (SAW) technology.

Can NanoVibronix devices be used at home?

Yes, NanoVibronix devices can be administered at home without professional assistance.

Last updated: Nov 21, 2023