Soterix Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
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) cleared devices by Soterix Medical, Inc.
6 devices
Cleared
Feb 20, 2026
SPRY TMS Therapy System (0550)
Neurology
267d
Cleared
Jun 03, 2024
Milieve (YPS-301BD)
Neurology
194d
Cleared
Mar 25, 2024
MEGA-IOM system with Neuro-IOM.NET software (32/B - 32/S - 16/S)
Neurology
94d
Cleared
Aug 13, 2021
MEGA-TMS
Neurology
681d
Cleared
Apr 06, 2020
Neural Navigator
Neurology
313d
Cleared
May 01, 2017
IontoDC
Physical Medicine
90d