ENvue Medical Launches Program to Address Patient Pain and Discomfort with Indwelling Nasogastric Tubes Based on Previously Published, Peer-Reviewed Clinical Research
Rhea-AI Summary
ENvue Medical (NASDAQ: FEED) launched a development and integration program to evaluate its clinically validated NanoVibronix vibration technology for reducing pain and discomfort from indwelling nasogastric (NG) tubes.
The program builds on previously published, peer‑reviewed research showing surface acoustic wave micro‑vibration can reduce friction at the tube–tissue interface. The effort is exploratory and focused on technical feasibility, clinical pathway assessment, and regulatory and quality considerations, and does not represent a commercial product launch or regulatory clearance.
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No peer stocks in the provided sector list showed momentum flags, suggesting today’s move is company-specific rather than sector-driven.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Jan 08 | Visibility event | Positive | +11.1% | Nasdaq Opening Bell ceremony highlighting enteral access and pain management focus. |
| Dec 15 | Leadership change | Positive | -5.6% | Appointment of experienced healthcare executive as Chairman to support expansion plans. |
Recent news showed mixed alignment: a leadership change saw a negative reaction, while a visibility-focused event aligned with a strong gain.
Over recent weeks, ENvue Medical issued visibility and leadership updates. On Dec 15, 2025, the appointment of a veteran healthcare executive as Chairman coincided with a -5.61% move, indicating a divergence between positive governance news and price. On Jan 8, 2026, the Nasdaq Opening Bell announcement aligned with an 11.11% gain, showing that profile-raising events have recently coincided with upside. Today’s program launch fits a pattern of strategic positioning in enteral care and patient comfort.
Market Pulse Summary
This announcement outlines an exploratory integration of NanoVibronix vibration-based technology to improve comfort for patients with indwelling nasogastric tubes, without constituting a commercial launch or regulatory clearance. It builds on previously published, peer-reviewed research suggesting benefits at the tube–tissue interface. Recent history shows ENvue balancing visibility events and leadership changes as it advances non-invasive enteral care. Investors may watch for concrete technical feasibility results, clinical pathway decisions, and any future moves to translate this program into regulated, commercial products.
Key Terms
nasogastric tubes medical
indwelling medical
enteral care medical
surface acoustic wave medical
micro-vibration technology technical
regulatory clearance regulatory
clinical pathway medical
AI-generated analysis. Not financial advice.
The program will integrate the Company’s clinically validated NanoVibronix technology to improve comfort associated with indwelling nasogastric tubes
TYLER, Texas, Jan. 09, 2026 (GLOBE NEWSWIRE) -- ENvue Medical, Inc. (NASDAQ: FEED) (NASDAQ: NAOV) (“ENvue,” “ENvue Medical” or the “Company”), a medical technology company specializing on the advancement of intelligent, non-invasive solutions for enteral care across clinical and home care settings, today announced the launch of a new development and integration program leveraging vibration-based technology from its NanoVibronix division to address pain and discomfort associated with indwelling nasogastric (NG) tubes.
Nasogastric tubes are among the most widely used devices in hospital care and are frequently required to remain in place for extended periods. While clinically essential, indwelling NG tubes are commonly associated with nasal and throat discomfort during the dwell phase, an issue for which limited mitigation options currently exist.¹,²,³
The newly launched program builds on previously published, peer-reviewed clinical research (link to full publication) demonstrating that surface acoustic wave micro-vibration technology applied to nasogastric tubes can reduce friction at the tube–tissue interface during indwelling use.4
Doron Besser, MD, CEO of ENvue Medical, commented, “We believe that this program represents a disciplined platform expansion initiative focused on improving the overall enteral care experience by addressing patient comfort during prolonged NG tube use. While this initiative is exploratory in nature and does not represent a commercial product launch or regulatory clearance announcement, we believe the data will be invaluable for our ongoing commercial efforts of our technology.”
Dr. Besser continued, “Enteral care does not end with accurate placement. This program reflects our strategy of responsibly extending the ENvue Platform to address clinically meaningful aspects of patient experience using validated technology we already own. This initiative aligns with our long-term strategy to expand beyond tube placement accuracy and support end-to-end enteral care, including workflow efficiency and patient experience, while maintaining capital discipline.”
The integration program will focus on technical feasibility, clinical pathway assessment, and regulatory and quality considerations to determine how vibration-based comfort technology could be incorporated into ENvue’s broader enteral ecosystem in the future.
References
1. Prabhakaran S. – Nasoenteric Tube Complications
Scand J Surg . 2012;101(3):147-55.
2. Singer AJ et al. – Pain experienced with Nasogastric Intubation
Ann Emerg Med 1999 Jun;33(6):652-8
3. StatPearls Publishing. Nasogastric Intubation. U.S. National Library of Medicine / NCBI Bookshelf.
4. Schlager A, Metzger YC, Adler SN. Use of surface acoustic waves to reduce pain and discomfort related to indwelling nasogastric tube. Endoscopy. Published ahead of print 2010. DOI: 10.1055/s-0030-1255801.
About ENvue Medical, Inc.
ENvue Medical, Inc. (NASDAQ: FEED) is a medical technology company specializing on the advancement of intelligent, non-invasive solutions for enteral care across clinical and home care settings. Headquartered in Tyler, Texas, with research and development in Tel-Aviv and Nesher, Israel, the Company focuses on two distinct technology platforms:
- ENvue™ Navigation Platform, developed and operated by ENvue Medical Inc., with offices in Arlington Heights, Illinois, and Tel-Aviv, Israel, is a minimally invasive electromagnetic navigation system intended to assist clinicians in placing feeding tubes into the gastrointestinal tract. FDA 510(k) cleared for adult use, ENvue provides real-time bedside visualization of tube movement and supports informed decision-making during the placement procedure. Future platform expansion may include pediatric and vascular access applications.
- ENvue Medical aims to advance standards in non-invasive therapy and minimally invasive navigation, with a commitment to patient safety, clinical usability, and technology innovation across a range of healthcare environments.
- Acoustic-based therapeutic technologies, including PainShield® and UroShield®, which utilize proprietary low-intensity surface acoustic wave (SAW) technology. These devices are intended for use in home or care settings and are designed to treat pain, reduce bacterial colonization, and disrupt biofilms.
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. These forward-looking statements include, but are not limited to: statements regarding the adoption and implementation of ENvue Medical’s platforms, anticipated commercial expansion, growth, scalability, and implementation of ENvue Medical’s products, the success of ENvue’s programs, market interest in the Company’s technology, and future expectations for strategic growth. 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: (i) market acceptance of the Company’s existing and new products; (ii) clinical performance and operational outcomes; (iii) delays or complications in product implementation; (iv) intense competition in the medical device industry; (v) product liability or performance issues; (vi) limitations in manufacturing or supply chain capabilities; (vii) reimbursement limitations; (viii) intellectual property protection; (ix) healthcare regulatory changes in the U.S. and abroad; and (x) the need for additional capital. 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, Quarterly Reports on Form 10-Q, and Current Reports on Form 8-K. Investors and security holders are urged to read these documents free of charge at: 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.
Investor Contact:
KCSA Strategic Communications
Valter Pinto, Managing Director
PH: (212) 896-1254
envue@kcsa.com