Medical Device Manufacturer · US , St. Louis , MO

Omni Therm, Inc. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 1987

Total

Cleared

Denied

Omni Therm, Inc. has 4 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Historical record: 4 cleared submissions from 1987 to 1996. Primary specialty: Physical Medicine.

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

Omni Therm, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Omni Therm, Inc.

5 devices

1-5 of 5