NeurAxis, Inc. received a VA contract for its IB-Stim® device, improving access to treatment for veterans with abdominal pain.
Quiver AI Summary
NeurAxis, Inc. announced the awarding of a Veterans Affairs (VA) Federal Supply Schedule contract effective December 1, 2025, allowing the company to offer its drug-free treatment IB-Stim® for functional abdominal pain in patients 8 years and older within the VA health system. This contract positions NeurAxis as a federal contractor and opens a pathway to serve nearly 7 million active VA patients annually. The IB-Stim device, which is FDA-cleared and employs non-invasive neuromodulation, addresses a significant unmet medical need in treating conditions like irritable bowel syndrome and functional dyspepsia. With this VA contract and the anticipated introduction of a new clinical code in 2026, NeurAxis aims to enhance the adoption of its therapy and drive revenue growth, as it dedicates resources to expand its sales efforts within the VA system.
Potential Positives
- NeurAxis has been awarded a Veterans Affairs Federal Supply Schedule contract, enabling access to a significant customer base within the VA health system, which serves nearly 7 million active patients annually.
- The inclusion of the IB-Stim® device, a unique FDA-cleared therapy for functional abdominal pain, showcases NeurAxis' innovative approach to addressing an unmet medical need in patients aged 8 and older.
- The contract award is expected to drive sustained commercial momentum for NeurAxis entering 2026, supported by forthcoming clinical recognition and expanding reimbursement avenues.
- The anticipated impact of a Category I CPT code effective January 1, 2026, is likely to enhance the marketability and adoption of IB-Stim, positioning the company for revenue growth and margin expansion.
Potential Negatives
- The press release emphasizes the lack of FDA-approved drug therapies for functional dyspepsia, highlighting a significant gap in treatment options that may raise concerns about the effectiveness and market dependency on the IB-Stim device.
- The mention of "limited efficacy data and potential safety concerns" regarding off-label prescription drugs implies scrutiny and challenges surrounding existing treatments, which could affect confidence among investors and healthcare providers.
- The reliance on forward-looking statements carries inherent risks, as it indicates that actual results may differ materially from the company's expectations, potentially deterring investors concerned about the company's future performance.
FAQ
What is the significance of the VA Federal Supply Schedule contract for NeurAxis?
The contract establishes NeurAxis as a federal contractor, creating a commercial path into the VA health system.
What does the IB-Stim device treat?
IB-Stim is a drug-free treatment for functional abdominal pain associated with IBS and functional dyspepsia in patients aged 8 and older.
When does the CPT code for IB-Stim take effect?
The Category I CPT code for IB-Stim will take effect on January 1, 2026.
How does IB-Stim work?
IB-Stim gently stimulates cranial nerve bundles in the ear to help regulate pain signaling between the gut and the brain.
Why is IB-Stim unique in treating functional dyspepsia?
IB-Stim is the only FDA-cleared therapy for functional dyspepsia, addressing a significant unmet medical need.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$NRXS Insider Trading Activity
$NRXS insiders have traded $NRXS stock on the open market 2 times in the past 6 months. Of those trades, 0 have been purchases and 2 have been sales.
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$NRXS Analyst Ratings
Wall Street analysts have issued reports on $NRXS in the last several months. We have seen 1 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
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Full Release
CARMEL, Ind., Dec. 01, 2025 (GLOBE NEWSWIRE) -- NeurAxis, Inc. (“NeurAxis” or the “Company”) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies for chronic and debilitating conditions in children and adults, today announced that it has been awarded a Veterans Affairs (VA) Federal Supply Schedule (FSS) contract, effective December 1, 2025. The first product listed on the FSS is the IB-Stim ® , a drug-free treatment for functional abdominal pain in patients 8 years and older. This contract award establishes NeurAxis as a federal contractor and creates a clear commercial pathway into the VA health system, which serves nearly 7 million active patients annually. The Company expects the VA award, combined with broadening reimbursement and increasing clinical adoption, to support sustained commercial momentum entering 2026.
NeurAxis’ proprietary technology, IB-Stim, is an FDA-cleared percutaneous electrical nerve field stimulator (PENFS) for the treatment of functional abdominal pain associated with irritable bowel syndrome (IBS), functional dyspepsia (FD), and FD-related nausea symptoms in patients 8 years and older. IB-Stim is a non-invasive neuromodulation device that gently stimulates cranial nerve bundles in the ear to help regulate pain signaling between the gut and the brain. Currently, no FDA-approved drug therapies exist for functional dyspepsia, a significant unmet medical need in the care of both pediatric and adult patients. In the absence of approved options, off-label prescription drugs for functional dyspepsia are often used, despite limited efficacy data and potential safety concerns—underscoring IB-Stim’s unique position as the only FDA-cleared therapy for FD.
“We are pleased to expand access to IB-Stim for the hundreds of thousands of veterans suffering from functional abdominal pain and nausea due to FD,” said Brian Carrico, CEO of NeurAxis. “The VA contract award represents an important commercial milestone and supports our ongoing channel expansion strategy. With a Category I CPT code taking effect January 1, 2026, guideline-level clinical recognition, and a strengthened balance sheet, NeurAxis is well-positioned for meaningful revenue growth and margin expansion. We are dedicating sales resources to the VA and will scale our efforts as utilization grows.”
About NeurAxis, Inc.
NeurAxis, Inc., is a medical technology company focused on neuromodulation therapies to address chronic and debilitating conditions in children and adults. NeurAxis is dedicated to advancing science and leveraging evidence-based medicine to drive adoption of its IB-Stim
®
therapy, which is its proprietary percutaneous electrical nerve field stimulator (PENFS), by the medical, scientific, and patient communities. IB-Stim is FDA-cleared for functional abdominal pain associated with irritable bowel syndrome (IBS) and functional dyspepsia in patients 8 years and older. Additional clinical trials of PENFS in multiple pediatric and adult conditions with large unmet healthcare needs are underway. For more information, please visit
http://neuraxis.com
.
Forward-Looking Statements
Certain statements in this press release are 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. All statements other than statements of historical fact are forward-looking statements. Forward-looking statements are based on management’s current assumptions and expectations of future events and trends, which affect or may affect the Company’s business, strategy, operations or financial performance, and actual results and other events may differ materially from those expressed or implied in such statements due to numerous risks and uncertainties. Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified. There are a number of important factors that could cause actual results, developments, business decisions or other events to differ materially from those contemplated by the forward-looking statements in this press release. These factors include, among other things, the conditions in the U.S. and global economy, the trading price and volatility of the Company’s stock, public health issues or other events, the Company’s compliance with applicable laws, the results of the Company’s clinical trials and perceptions thereof, the results of submissions to the FDA, and factors described in the Risk Factors section of NeurAxis’s public filings with the Securities and Exchange Commission (SEC). Because forward-looking statements are inherently subject to risks and uncertainties, you should not rely on these forward-looking statements as predictions of future events. These forward-looking statements speak only as of the date of this press release and, except to the extent required by applicable law, the Company undertakes no obligation to update or revise these statements, whether as a result of any new information, future events and developments or otherwise.
Contacts:
Company
NeurAxis, Inc.
[email protected]
For contraindications, precautions, warnings, and IFU, please see:
https://ibstim.com/important-information/
.
Investor Relations
Lytham Partners
Ben Shamsian
646-829-9701
[email protected]