Medical Device Manufacturer · US , Lake Bluff , IL

Somatics, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1984

Total

Cleared

Denied

Somatics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lake Bluff, US.

Historical record: 7 cleared submissions from 1984 to 1999. Primary specialty: Neurology.

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

Somatics, Inc. is one of 14237 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Somatics, Inc.

7 devices

1-7 of 7