Neuraxis, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neuraxis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Carmel, US.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neuraxis, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Neuraxis, Inc.
1 devices