{"id":852716,"date":"2025-05-20T08:07:35","date_gmt":"2025-05-20T12:07:35","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/neuraxis-awarded-first-ever-fda-clearance-for-the-treatment-of-pediatric-fap-functional-dyspepsia-fd-and-associated-nausea-symptoms\/"},"modified":"2025-05-20T08:07:35","modified_gmt":"2025-05-20T12:07:35","slug":"neuraxis-awarded-first-ever-fda-clearance-for-the-treatment-of-pediatric-fap-functional-dyspepsia-fd-and-associated-nausea-symptoms","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/neuraxis-awarded-first-ever-fda-clearance-for-the-treatment-of-pediatric-fap-functional-dyspepsia-fd-and-associated-nausea-symptoms\/","title":{"rendered":"NeurAxis Awarded First Ever FDA Clearance for the Treatment of Pediatric FAP\/Functional Dyspepsia (FD) and Associated Nausea Symptoms"},"content":{"rendered":"
\n

\n \u2022\u00a0 \u00a0Significantly expands IB-Stim\u2019s total addressable market<\/em>\n <\/p>\n

\n \u2022\u00a0 \u00a0Clearance covers patients aged 8\u201321<\/em>\n <\/p>\n

\n \u2022\u00a0 \u00a0Seamless go-to-market strategy with existing reimbursement and provider infrastructure<\/em>\n <\/p>\n

CARMEL, Ind., May 20, 2025 (GLOBE NEWSWIRE) — NeurAxis, Inc. (\u201cNeurAxis,\u201d or the \u201cCompany\u201d) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies addressing chronic and debilitating conditions in children and adults, today announced that it has received FDA 510(k) clearance for IB-Stim\u2122 for the treatment of Pediatric Functional Abdominal Pain (FAP) associated with Functional Dyspepsia, and FD related Nausea Symptoms, in patients aged 8 to 21 years. This clearance is the second successful expanded FDA indication for IB-Stim, following its initial approval for Functional Abdominal Pain associated with Irritable Bowel Syndrome (IBS). The new indication represents the first treatment ever cleared or approved by the FDA related to functional dyspepsia. It is expected to nearly double the Company\u2019s total addressable market, reinforcing NeurAxis\u2019 leadership in non-invasive, pediatric-focused neuromodulation.<\/p>\n

The indication leverages the same CPT code, insurance coverage, and provider call points as the existing IBS indication, supporting a seamless and capital-efficient go-to-market strategy. Commercial rollout for this expanded important indication will begin immediately.<\/p>\n

\u201cThis latest FDA clearance represents a pivotal milestone in NeurAxis\u2019 growth strategy,\u201d said Brian Carrico, President and Chief Executive Officer of NeurAxis. \u201cExpanding into the treatment of Pediatric Functional Dyspepsia pain that includes related nausea symptoms, not only broadens our clinical impact but also positions us to drive significant revenue growth through a capital-efficient rollout. This progress is fueled by a robust body of clinical evidence supporting our PENFS technology, which continues to gain traction among providers and payers. Notably, we are seeing expanded insurance coverage and, most recently, the American Medical Association\u2019s approval of a new CPT Category I code for IB-Stim, which will take effect in January 2026.\u201d<\/p>\n

\u201cFunctional dyspepsia can cause severe abdominal pain and nausea, and in adolescents, it often leads to serious secondary issues like fear of eating, weight loss, and significant dietary restriction,\u201d said Dr. Adrian Miranda, Chief Medical Officer of NeurAxis. \u201cWe are thrilled by the agency\u2019s decision, which gives us the opportunity to offer real hope to thousands of patients and their families who have had limited options\u2014until now.\u201d<\/p>\n

NeurAxis\u2019 PENFS technology, IB-Stim, is FDA-cleared for functional abdominal pain associated with irritable bowel syndrome (IBS) and Functional Dyspepsia in adolescents 8-21 years old. IB-Stim is a non-surgical device that sends gentle electrical impulses into cranial nerve bundles in the ear. There are currently no FDA-approved drug therapies for children with abdominal pain-related disorders of the gut-brain interaction (DGBI\u2019s). Pharmacologic treatments that use drugs off-label can often have serious side effects, and most lack scientific evidence of efficacy.<\/p>\n

\n About NeurAxis, Inc.<\/strong>
\n
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\u2122 therapy, which is its proprietary Percutaneous Electrical Nerve Field Stimulation (PENFS) technology, by the medical, scientific, and patient communities. IB-Stim\u2122 is FDA cleared for functional abdominal pain associated with irritable bowel syndrome (IBS) in adolescents 8-21 years old. Additional clinical trials of PENFS in multiple pediatric and adult conditions with large unmet healthcare needs are underway. For more information, please visit\u00a0http:\/\/neuraxis.com<\/a>.<\/p>\n

\n Forward-Looking Statements <\/strong>
\n
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\u2019s current assumptions and expectations of future events and trends, which affect or may affect the Company\u2019s 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\u2019s stock, public health issues or other events, the Company\u2019s compliance with applicable laws, the results of the Company\u2019s clinical trials and perceptions thereof, the results of submissions to the FDA, the results of the shareholder vote to enable the issuance of the Preferred Stock, and factors described in the Risk Factors section of NeurAxis\u2019s 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.<\/p>\n

\n For Contraindications, Precautions, Warnings, and IFU, please see: <\/strong>
\n
\n https:\/\/ibstim.com\/important-information\/<\/strong>
\n <\/a>\n <\/p>\n

\n Contacts:<\/strong>\n <\/p>\n

\n Company<\/strong>
\n
\n NeurAxis, Inc.<\/strong>
\n
info@neuraxis.com<\/p>\n

\n Investor Relations<\/strong>
\n
Lytham Partners
Ben Shamsian
646-829-9701
shamsian@lythampartners.com<\/a><\/p>\n

\"\"
\n
\n \"\"\n <\/div>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

\u2022\u00a0 \u00a0Significantly expands IB-Stim\u2019s total addressable market \u2022\u00a0 \u00a0Clearance covers patients aged 8\u201321 \u2022\u00a0 \u00a0Seamless go-to-market strategy with existing reimbursement and provider infrastructure CARMEL, Ind., May 20, 2025 (GLOBE NEWSWIRE) — NeurAxis, Inc. (\u201cNeurAxis,\u201d or the \u201cCompany\u201d) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies addressing chronic and debilitating conditions in children and adults, today announced that it has received FDA 510(k) clearance for IB-Stim\u2122 for the treatment of Pediatric Functional Abdominal Pain (FAP) associated with Functional Dyspepsia, and FD related Nausea Symptoms, in patients aged 8 to 21 years. This clearance is the second successful expanded FDA indication for IB-Stim, following its initial approval for Functional Abdominal Pain associated with Irritable Bowel Syndrome (IBS). The new indication … <\/p>\n

Continue reading “NeurAxis Awarded First Ever FDA Clearance for the Treatment of Pediatric FAP\/Functional Dyspepsia (FD) and Associated Nausea Symptoms”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-852716","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nNeurAxis Awarded First Ever FDA Clearance for the Treatment of Pediatric FAP\/Functional Dyspepsia (FD) and Associated Nausea Symptoms - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/neuraxis-awarded-first-ever-fda-clearance-for-the-treatment-of-pediatric-fap-functional-dyspepsia-fd-and-associated-nausea-symptoms\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"NeurAxis Awarded First Ever FDA Clearance for the Treatment of Pediatric FAP\/Functional Dyspepsia (FD) and Associated Nausea Symptoms - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"\u2022\u00a0 \u00a0Significantly expands IB-Stim\u2019s total addressable market \u2022\u00a0 \u00a0Clearance covers patients aged 8\u201321 \u2022\u00a0 \u00a0Seamless go-to-market strategy with existing reimbursement and provider infrastructure CARMEL, Ind., May 20, 2025 (GLOBE NEWSWIRE) — NeurAxis, Inc. (\u201cNeurAxis,\u201d or the \u201cCompany\u201d) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies addressing chronic and debilitating conditions in children and adults, today announced that it has received FDA 510(k) clearance for IB-Stim\u2122 for the treatment of Pediatric Functional Abdominal Pain (FAP) associated with Functional Dyspepsia, and FD related Nausea Symptoms, in patients aged 8 to 21 years. This clearance is the second successful expanded FDA indication for IB-Stim, following its initial approval for Functional Abdominal Pain associated with Irritable Bowel Syndrome (IBS). 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(\u201cNeurAxis,\u201d or the \u201cCompany\u201d) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies addressing chronic and debilitating conditions in children and adults, today announced that it has received FDA 510(k) clearance for IB-Stim\u2122 for the treatment of Pediatric Functional Abdominal Pain (FAP) associated with Functional Dyspepsia, and FD related Nausea Symptoms, in patients aged 8 to 21 years. This clearance is the second successful expanded FDA indication for IB-Stim, following its initial approval for Functional Abdominal Pain associated with Irritable Bowel Syndrome (IBS). 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