Medical Device Manufacturer · US , Washington D.C. , DC

Tria Beauty, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2010

Total

Cleared

Denied

Tria Beauty, Inc. has 5 FDA 510(k) cleared medical devices. Based in Washington D.C., US.

Historical record: 5 cleared submissions from 2010 to 2016. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Tria Beauty, Inc. is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tria Beauty, 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 17, 2026