Medical Device Manufacturer · US , Woodbridge , NJ

Soterix Medical, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2017

Total

Cleared

Denied

Soterix Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Woodbridge, US.

Latest FDA clearance: Feb 2026. Active since 2017. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Soterix Medical, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Soterix Medical, Inc.

6 devices

1-6 of 6