NeuroOne® Regains Compliance with Nasdaq Listing Requirements
NeuroOne Medical Technologies (Nasdaq: NMTC) has regained compliance with Nasdaq Capital Market's continued listing requirements for minimum share price under Rule 5550(a)(2). The company received confirmation from Nasdaq's Listings Qualifications Hearing Department on February 3, 2025, resulting in the cancellation of a previously scheduled hearing.
The company also reported preliminary unaudited first quarter fiscal 2025 total revenue of $6.2 million, comprising $3.2 million in product revenue and a one-time $3.0 million license revenue payment. NeuroOne's CEO Dave Rosa highlighted the company's focus on their OneRF Ablation System, which is the first and only FDA-cleared device for RF ablation in the brain. The company will provide further updates during their upcoming earnings call scheduled for February 12, 2025, at 8:30 am eastern time.
NeuroOne Medical Technologies (Nasdaq: NMTC) ha riacquistato la conformità ai requisiti di quotazione continue del Nasdaq Capital Market per il prezzo minimo delle azioni ai sensi della Regola 5550(a)(2). L'azienda ha ricevuto conferma dal Dipartimento delle Qualifiche per le Quotazioni del Nasdaq il 3 febbraio 2025, portando alla cancellazione di un'udienza precedentemente programmata.
L'azienda ha anche riportato un fatturato totale preliminare non verificato per il primo trimestre dell'esercizio fiscale 2025 di 6,2 milioni di dollari, di cui 3,2 milioni di dollari provenienti da ricavi da prodotti e un pagamento una tantum di 3,0 milioni di dollari da licenze. Il CEO di NeuroOne, Dave Rosa, ha sottolineato il focus dell'azienda sul loro OneRF Ablation System, che è il primo e unico dispositivo approvato dalla FDA per l'ablazione RF nel cervello. L'azienda fornirà ulteriori aggiornamenti durante la prossima chiamata sugli utili programmata per il 12 febbraio 2025, alle 8:30 ora orientale.
NeuroOne Medical Technologies (Nasdaq: NMTC) ha recuperado el cumplimiento de los requisitos de cotización continua del Nasdaq Capital Market para el precio mínimo de las acciones según la Regla 5550(a)(2). La compañía recibió la confirmación del Departamento de Calificaciones de Listado del Nasdaq el 3 de febrero de 2025, lo que resultó en la cancelación de una audiencia previamente programada.
La empresa también reportó ingresos totales preliminares no auditados para el primer trimestre del año fiscal 2025 de 6.2 millones de dólares, que incluyen 3.2 millones de dólares en ingresos por productos y un pago único de 3.0 millones de dólares en ingresos por licencias. El CEO de NeuroOne, Dave Rosa, destacó el enfoque de la compañía en su Sistema de Ablación OneRF, que es el primer y único dispositivo aprobado por la FDA para la ablación por RF en el cerebro. La compañía proporcionará más actualizaciones durante su próxima llamada de ganancias programada para el 12 de febrero de 2025, a las 8:30 am hora del este.
뉴로원 메디컬 테크놀로지스 (Nasdaq: NMTC)는 규칙 5550(a)(2)에 따른 최소 주가에 대한 나스닥 자본 시장의 지속적 상장 요구 사항을 준수하게 되었습니다. 회사는 2025년 2월 3일 나스닥 상장 자격 심사 부서로부터 확인을 받았으며, 이로 인해 이전에 예정되었던 청문회가 취소되었습니다.
회사는 또한 2025 회계 연도 1 분기의 비검토 총 수익이 620만 달러로, 제품 수익이 320만 달러, 일회성 면허 수익이 300만 달러로 구성되어 있다고 보고했습니다. 뉴로원의 CEO 데이브 로사는 회사의 뇌 RF 절제에 대한 FDA 승인이 된 첫 번째이자 유일한 장치인 OneRF 절제 시스템에 집중하고 있음을 강조했습니다. 회사는 2025년 2월 12일 동부 표준시 기준 오전 8:30에 예정된 다음 수익 발표 전화 회의에서 추가 업데이트를 제공할 예정입니다.
NeuroOne Medical Technologies (Nasdaq: NMTC) a regagné la conformité aux exigences de cotation continue du Nasdaq Capital Market concernant le prix minimum des actions selon la règle 5550(a)(2). La société a reçu une confirmation du département des qualifications de cotation du Nasdaq le 3 février 2025, ce qui a entraîné l'annulation d'une audience précédemment prévue.
La société a également signalé des revenus totaux préliminaires non audités pour le premier trimestre de l'exercice fiscal 2025 s'élevant à 6,2 millions de dollars, comprenant 3,2 millions de dollars de revenus de produits et un paiement unique de 3,0 millions de dollars de revenus de licences. Le PDG de NeuroOne, Dave Rosa, a souligné l'importance pour l'entreprise de son système d'ablation OneRF, qui est le premier et unique dispositif approuvé par la FDA pour l'ablation RF dans le cerveau. L'entreprise fournira d'autres mises à jour lors de sa prochaine conférence sur les résultats prévue pour le 12 février 2025 à 8h30, heure de l'Est.
NeuroOne Medical Technologies (Nasdaq: NMTC) hat die Einhaltung der fortlaufenden Zulassungsvoraussetzungen des Nasdaq Capital Market für den Mindestaktienkurs gemäß Regel 5550(a)(2) wiederhergestellt. Das Unternehmen erhielt am 3. Februar 2025 eine Bestätigung von der Abteilung für Zulassungsqualifikationen des Nasdaq, was zur Streichung einer zuvor angesetzten Anhörung führte.
Das Unternehmen berichtete auch über vorläufige nicht testierte Gesamterlöse für das erste Quartal des Geschäftsjahres 2025 in Höhe von 6,2 Millionen US-Dollar, bestehend aus 3,2 Millionen US-Dollar aus Produktverkäufen und einer einmaligen Lizenzgebühr von 3,0 Millionen US-Dollar. Der CEO von NeuroOne, Dave Rosa, hob den Fokus des Unternehmens auf ihr OneRF Ablationssystem hervor, das das erste und einzige von der FDA zugelassene Gerät für RF-Ablation im Gehirn ist. Das Unternehmen wird während des bevorstehenden Earnings-Calls, der für den 12. Februar 2025 um 8:30 Uhr Eastern Time angesetzt ist, weitere Updates bereitstellen.
- Regained Nasdaq listing compliance, eliminating delisting risk
- Record quarterly revenue of $6.2 million in Q1 FY2025
- First and only FDA-cleared RF ablation device for brain procedures
- One-time license payment of $3.0M accounts for nearly half of Q1 revenue
Insights
The announcement of NeuroOne regaining Nasdaq compliance marks a important turning point for the company, eliminating a significant overhang that typically constrains small-cap medical technology stocks. This development is particularly noteworthy when coupled with the company's record preliminary Q1 FY2025 revenue of
The revenue composition reveals important insights: product revenue of
The timing of these announcements, coming just before their February 12 earnings call, positions NeuroOne to build positive momentum. The company's focus on the OneRF Ablation System, being the first FDA-cleared device for RF ablation in the brain, gives them a first-mover advantage in a specialized market segment. This regulatory clearance and market position create significant barriers to entry, potentially supporting sustained growth in their product revenue stream.
EDEN PRAIRIE, Minn., Feb. 04, 2025 (GLOBE NEWSWIRE) -- NeuroOne Medical Technologies Corporation (Nasdaq: NMTC) ("NeuroOne" or the "Company"), a medical technology company focused on improving surgical care options and outcomes for patients suffering from neurological disorders, today announced that it has regained compliance with the Nasdaq Capital Market’s continued listing standard for the minimum share price requirements under Nasdaq Listing Rule 5550(a)(2).
The Company received a letter on February 3, 2025 from the Listings Qualifications Hearing Department of Nasdaq that the Company’s bid price deficiency had been cured and that the Company was in compliance with all applicable listing standards.
Based on the foregoing, the previously scheduled Nasdaq hearing has been cancelled and the matter is now closed.
“We are pleased to announce that we have regained compliance with Nasdaq’s share price listing standards and are grateful to our shareholders for their patience during this time,” said Dave Rosa, Chief Executive Officer of NeuroOne. “We remain focused on driving sustainable shareholder value over the long term as we successfully penetrate the market with our disruptive OneRF Ablation System, the first and only FDA-cleared device for RF ablation in the brain. Following our recent announcement that preliminary unaudited first quarter fiscal 2025 total revenue increased to a record
About NeuroOne
NeuroOne Medical Technologies Corporation (Nasdaq: NMTC) is developing and commercializing minimally invasive and hi-definition solutions for EEG recording, brain stimulation and ablation solutions for patients suffering from epilepsy, Parkinson’s disease, dystonia, essential tremors, chronic pain due to failed back surgeries and other related neurological disorders that may improve patient outcomes and reduce procedural costs. The Company may also pursue applications for other areas such as depression, mood disorders, pain, incontinence, high blood pressure, and artificial intelligence. For more information, visit nmtc1.com.
Forward Looking Statements
This press release may include forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Except for statements of historical fact, any information contained in this press release may be a forward–looking statement that reflects NeuroOne’s current views about future events and are subject to known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. In some cases, you can identify forward–looking statements by the words or phrases “may,” “might,” “will,” “could,” “would,” “should,” “expect,” “intend,” “plan,” “forecasts,” “objective,” “anticipate,” “believe,” “estimate,” “predict,” “project,” “potential,” “target,” “seek,” “contemplate,” “continue, “focused on,” “committed to” and “ongoing,” or the negative of these terms, or other comparable terminology intended to identify statements about the future. Our actual future results may be materially different from what we expect due to factors largely outside our control, including risks related to whether the Company will continue to maintain compliance with all Nasdaq continued listing requirements; and other risks, uncertainties and assumptions, including those described under the heading “Risk Factors” in our filings with the Securities and Exchange Commission. These forward–looking statements speak only as of the date of this press release and NeuroOne undertakes no obligation to revise or update any forward–looking statements for any reason, even if new information becomes available in the future.
Caution: Federal law restricts this device to sale by or on the order of a physician.
IR Contact
MZ Group – MZ North America
NMTC@mzgroup.us
FAQ
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