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Vivos Therapeutics Announces Issuance of New US Patent Broadening Protection for Its Vivos CARE Oral Medical Device Technology

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Vivos Therapeutics (NASDAQ: VVOS) announced that the US Patent and Trademark Office has issued US Patent No. 12,697,190, titled “Vibrational Oral Appliance with Mandibular Advancements.” This continuation of the 2024 foundational Patent No. 12,048,608 broadens protection for the company’s Vivos CARE vibrational oral appliance platform.

The ’190 Patent adds broader, design‑independent claims while the ’608 Patent maintains detailed, structure‑specific coverage, giving Vivos layered intellectual property protection around its core technology. According to Vivos, its CARE oral devices are the only FDA 510(k) cleared oral appliances for treating severe OSA in adults and moderate to severe OSA in children ages 6–17. Studies cited by the company indicate that about 80% of patients treated with Vivos CARE devices achieve significant reductions or complete resolution of OSA symptoms, measured by standard AHI scores. Vivos believes this expanded patent estate strengthens its competitive position in a large, underdiagnosed global sleep apnea market.

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Positive

  • New US continuation patent ’190 broadens Vivos CARE oral device IP protection
  • Two FDA 510(k) clearances for treating severe adult OSA and moderate–severe pediatric OSA
  • ~80% of Vivos CARE patients show significant AHI-based OSA symptom reduction or resolution, per studies cited

Negative

  • None.

Market reaction after US patent issuance: VVOS -26.31% in the Aug 5 session

-26.31% 4.2x vol
50 alerts
-26.31% Session close to close
+19.7% Peak Tracked
-14.7% Trough Tracked
$6.04M Market Cap
4.2x Rel. Volume

In the Aug 5 session, VVOS declined 26.31%, reflecting a significant negative market reaction. Argus tracked a peak move of +19.7% during that session. Argus tracked a trough of -14.7% from its starting point during tracking. Our momentum scanner triggered 50 alerts that day, indicating high trading interest and price volatility. Trading volume was very high at 4.2x the daily average, suggesting heavy selling pressure.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock dropped -26.3% in the session following this news. Historical context recorded a -19.56% 2...
Analysis

The stock dropped -26.3% in the session following this news. Historical context recorded a -19.56% 24-hour reaction after the June 22 financing-agreement update. VVOS also has an active S-3/A resale registration, with no company proceeds from selling-stockholder sales.

Key Figures

New patent number: 12,697,190 Foundational patent number: 12,048,608 FDA clearances: 2 separate 510(k) clearances +5 more
8 metrics
New patent number 12,697,190 US continuation patent issued August 5, 2026
Foundational patent number 12,048,608 US patent issued July 30, 2024
FDA clearances 2 separate 510(k) clearances Granted in 2023 and 2024
Patients with improvement Approximately 80% Vivos CARE device studies; significant reduction or resolution of OSA symptoms
CPAP units recalled Over 5 million units FDA-mandated recalls since 2021
Global sleep apnea sufferers More than 1 billion people Global population cited in the article
US sleep apnea sufferers Up to 90 million Americans Population cited in the article
Pediatric age range Ages 6-17 Children covered by one FDA clearance

Historical Context

5 past events · Latest: Jun 30 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 30 Clinical study results Positive -7.8% Insomnia scores improved across all 37 study participants, but shares declined 7.81%.
Jun 22 Financing agreement Negative -19.6% Debt conversion remained contingent on a $2.6 million equity raise and shares declined 19.56%.
Jun 11 Rights offering Negative -3.9% The proposed rights offering introduced potential equity issuance and shares declined 3.94%.
Jun 10 Collaboration agreement Positive -8.8% Vivos announced an 80% ownership position in AIM Florida, but shares declined 8.75%.
Jun 08 Investor presentation Neutral +0.6% Management scheduled a June 9 investor presentation and shares changed 0.64%.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

VVOS declined after two positive announcements, while financing and offering-related news also produced negative 24-hour reactions.

Key Terms

osa, 510(k), cpap
3 terms
osa medical
"patients suffering from obstructive sleep apnea (“OSA”)"
Obstructive sleep apnea (OSA) is a common sleep disorder where the upper airway repeatedly narrows or collapses during sleep, causing brief breathing stoppages that fragment rest and raise daytime tiredness and health risks. For investors, OSA creates sustained demand for diagnostic tests, therapy devices, drugs and monitoring services, so changes in clinical data, approvals, or reimbursement can materially affect revenue prospects for companies in the sleep-health sector.
510(k) regulatory
"the FDA granted two separate and unprecedented 510K clearances"
A 510(k) is a U.S. regulatory submission that a medical device maker uses to show a new device is as safe and effective as an already-approved device, allowing the regulator to clear it for sale rather than requiring the longer, more stringent approval process. For investors, a cleared 510(k) usually means lower regulatory risk and a faster path to market, which can speed revenue generation and reduce uncertainty—similar to proving a new appliance works like a trusted existing model.
cpap medical
"increased mortality and health risks associated with CPAP"
A CPAP (continuous positive airway pressure) device is a machine that gently blows a steady stream of air through a mask to keep a person’s breathing passages open during sleep, commonly used to treat sleep apnea. For investors, CPAPs matter because they represent a medical-device market with recurring sales of equipment and disposable supplies, subject to safety reviews, insurance reimbursement rules and regulatory approvals that can affect a maker’s revenue and reputation.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Continuation Patent Secures Broader, Design Independent Claims, Building on the Company's 2024 Foundational Patent for Its Vibrational Oral Appliance Platform

LITTLETON, Colo., Aug. 05, 2026 (GLOBE NEWSWIRE) -- Vivos Therapeutics, Inc. (“Vivos” or “the Company”) (NASDAQ: VVOS), a leading medical device and healthcare services company focused on developing and commercializing innovative diagnostic and treatment modalities for patients suffering from obstructive sleep apnea (“OSA”) and other sleep related breathing disorders, today announced that the United States Patent and Trademark Office has issued US Patent No. 12,697,190 “Vibrational Oral Appliance with Mandibular Advancements” (the “’190 Patent”), a continuation of the Company’s previously issued US Patent No. 12,048,608 (the “’608 Patent”), issued July 30, 2024.

Taken together, these two patents broaden the patent protections around Vivos’ proprietary line of oral medical devices known as Vivos CARE devices. In 2023 and 2024, the FDA granted two separate and unprecedented 510K clearances for these devices to treat severe OSA in adults and moderate to severe OSA in children (ages 6-17). To date, no other oral appliances have ever received such clearances from the FDA. Studies have shown that approximately 80% of patients treated with Vivos CARE devices achieve significant reductions or complete resolution of OSA symptoms (as measured by industry standard AHI scores).

Given the recently discovered and documented increased mortality and health risks associated with CPAP, and the massive FDA-mandated recalls of over 5 million CPAP units since 2021, the clinical and commercial market for a safe and highly effective alternative technology to treat the more severe forms of OSA has never been brighter. The Company believes that broadening the patent protections afforded by this new continuation patent will strengthen its industry-leading position and technological advantages.

The newly issued ’190 Patent broadens the scope of protection first established by the ’608 Patent, giving Vivos layered, complementary coverage over the underlying Vivos technology.   The ’608 Patent's more detailed, structure-specific claims remain valuable and in force, providing focused protection for that particular design embodiment. Together, the two patents give Vivos broad, difficult-to-design-around protection and detailed, embodiment-specific protection over its core technology.

Commenting on the newly issued patent, Vivos Chairman and CEO Kirk Huntsman stated, “We believe this new patent meaningfully strengthens our intellectual property position around the technology at the heart of our most important and advanced product lines. Broader, more resilient patent claims make it harder for competitors to design around our innovations, and they reflect the continued investment we're making in protecting the science behind better outcomes for patients suffering from OSA.”

More than one billion people globally and up to 90 million Americans suffer from sleep apnea, 80 percent of whom remain undiagnosed. A serious chronic illness, sleep apnea increases the risk of comorbidities, including high blood pressure, heart failure, stroke, diabetes, dementia, chronic pain, fibromyalgia, and other life-threatening diseases.

About Vivos Therapeutics, Inc.

Vivos Therapeutics, Inc. (Nasdaq: VVOS) is a medical technology and healthcare services company focused on developing and commercializing innovative diagnostic and treatment methods for patients suffering from breathing and sleep issues arising from certain dentofacial abnormalities such as obstructive sleep apnea (OSA) and snoring in adults. Vivos’ devices have been cleared by the U.S. Food and Drug Administration (FDA) for adult patients diagnosed with all severity levels of OSA and moderate-to-severe OSA in children ages 6 to 17. Vivos’ groundbreaking Complete Airway Repositioning and Expansion (CARE) devices are the only FDA 510(k) cleared technology for treating severe OSA in adults and the flagship DNA appliance is the first to receive clearance for treating moderate to severe OSA in children. 

OSA and insomnia affect over 1 Billion adults aged 30-69 years old worldwide, yet 80% or more remain undiagnosed and unaware of their condition. These chronic disorders are not just a sleep issue—they are closely linked to many serious chronic health conditions. While the medical community has made strides in treating sleep disorders, breathing and sleep health remain areas that are still not fully understood. As a result, legacy OSA treatments like CPAP are often mechanistic and fail to address the root causes. Vivos CARE oral medical devices target the underlying physiology and anatomical deficiencies that are often associated with OSA.

Through innovative technology, education, and acquisitions of, or commercial collaborations with, sleep healthcare providers, Vivos is empowering healthcare providers to address the complex needs of OSA patients more thoroughly.

Vivos calls the use of its appliances and protocols to treat OSA The Vivos Method, which offers a proprietary, clinically effective solution that is nonsurgical, noninvasive, and nonpharmaceutical, providing hope to allow patients to Breathe New Life.

For more information, visit www.vivos.com.

Cautionary Note Regarding Forward‑Looking Statements

This press release, including statements of the Company's management and other parties made in connection therewith, contains "forward-looking statements" (as defined in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended) concerning future events. Words such as "may," "would," "should," "expects," "projects," "potential," "intends," "plans," "believes," "anticipates," "hopes," "estimates," "goal," "aim," and variations of such words and similar expressions are intended to identify forward-looking statements. In this press release, forward-looking statements include, without limitation, statements regarding: the scope, breadth, enforceability, and durability of the claims of the ’190 Patent and the ’608 Patent, and the layered, complementary protection the two patents together are expected to provide; the extent to which the ’190 Patent may make it more difficult for competitors to design around the Company’s mandibular advancement technology; the potential for the patented technology to promote jaw and palate development and to provide relief from breathing and sleep disorders, sleep apnea, and snoring; the strengthening of the Company’s intellectual property position with respect to the technology underlying certain of the Company’s product lines; the Company’s continued investment in protecting its intellectual property; and the potential impact of the foregoing on the Company’s competitive position, product lines, revenues, and overall growth.

These statements involve significant known and unknown risks and are based upon a number of assumptions and estimates that are inherently subject to significant uncertainties and contingencies, many of which are beyond Vivos' control. Actual results may differ materially and adversely from those expressed or implied by such forward-looking statements as a result of various factors, including, but not limited to: (i) the risk that the newly issued continuation patent described herein may be of limited practical value in terms of its ability to protect the intellectual property and claims covered therein; (ii) the risk that the ’190 Patent or the ’608 Patent may be challenged, invalidated, narrowed in scope, circumvented, or held unenforceable, or that the Company may not be successful in enforcing or defending such patents against third parties; (iii) the risk that new or competing technology may limit or extinguish the new patent’s economic value to the Company; (iv) the risk that Vivos may be unable to effectively market the products covered by the new patent or otherwise implement strategies that increase revenues; (v) risks associated with regulatory scrutiny of, and adverse publicity in, the sleep apnea and sleep disorder diagnosis and treatment sector; (vi) the risk that Vivos may be unable to secure additional financing to continue operations, acquire or affiliate with additional sleep center practices, or maintain its Nasdaq listing, when needed, if at all; (vii) market and other conditions that could impact Vivos' business or ability to obtain financing; and (viii) other risk factors described in Vivos' filings with the Securities and Exchange Commission (the "SEC"), which are available free of charge on the SEC's website at www.sec.gov.

Except to the extent required by law, Vivos expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Vivos' expectations with respect thereto or any change in events, conditions, or circumstances on which any such statement is based.

Vivos Investor Relations Contact:

Jennifer Hauser, Executive Assistant to the CEO
jhauser@vivoslife.com
720-927-3125


FAQ

What did Vivos Therapeutics (NASDAQ: VVOS) announce on August 5, 2026?

Vivos Therapeutics announced issuance of US Patent No. 12,697,190, expanding protection for its Vivos CARE vibrational oral appliance technology. According to Vivos, this continuation patent builds on its 2024 foundational patent to provide broader, design-independent coverage of its core sleep apnea treatment platform.

How does the new US Patent No. 12,697,190 benefit Vivos Therapeutics (VVOS) investors?

The new patent broadens intellectual property protection for Vivos’ CARE oral devices with layered, complementary coverage. According to Vivos, wider, harder-to-design-around claims strengthen its competitive moat around technology used to treat obstructive sleep apnea, which may support long-term commercial positioning in a large addressable market.

What is the relationship between Vivos’ 2024 ’608 Patent and the new ’190 Patent for VVOS?

The ’190 Patent is a continuation of the 2024 US Patent No. 12,048,608, adding broader claims. According to Vivos, the ’608 Patent keeps detailed, structure-specific protection while the ’190 Patent supplies design-independent coverage, together creating layered protection around Vivos CARE oral appliance technology.

What FDA clearances support Vivos CARE devices mentioned in the August 2026 VVOS patent news?

According to Vivos, its CARE devices received two FDA 510(k) clearances in 2023 and 2024. These cover treatment of severe obstructive sleep apnea in adults and moderate to severe OSA in children ages 6–17, and are described as unique among oral appliances for these indications.

How effective are Vivos CARE oral devices for treating obstructive sleep apnea, according to Vivos Therapeutics (VVOS)?

Vivos reports that about 80% of patients treated with CARE devices achieve significant reductions or complete resolution of OSA symptoms. According to Vivos, outcomes are measured using standard apnea-hypopnea index (AHI) scores, indicating meaningful clinical improvements in many treated adult and pediatric patients.

What market opportunity does Vivos Therapeutics (VVOS) target with its CARE oral appliance platform?

Vivos targets patients with obstructive sleep apnea and related breathing disorders, a large underdiagnosed population. According to Vivos, more than one billion people globally and up to 90 million Americans have sleep apnea, with roughly 80% undiagnosed, supporting long-term demand for effective treatment alternatives.

How do Vivos CARE devices differ from legacy CPAP treatments for OSA mentioned by VVOS?

Vivos CARE devices are oral appliances targeting underlying physiological and anatomical factors associated with OSA instead of providing mechanical airflow support. According to Vivos, its noninvasive, nonsurgical approach offers an alternative to CPAP machines for moderate to severe OSA where patients and providers seek different treatment options.