Medical Device Manufacturer · US , San Diego , CA

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

5 submissions · 5 cleared · Since 2008

Total

Cleared

Denied

Thermopeutix, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 5 cleared submissions from 2008 to 2013. Primary specialty: Cardiovascular.

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

Regulatory submissions have been managed by Tuv Sud America, Inc. and Regulatory Technology Services, LLC.

Thermopeutix, Inc. is one of 18961 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 16, 2026