Medical Device Manufacturer · US , Washington , DC

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

7 submissions · 6 cleared · Since 2014

Total

Cleared

Denied

Revmedx, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.

Latest FDA clearance: Nov 2025. Active since 2014. Primary specialty: General & Plastic Surgery.

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

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

Revmedx, Inc. is one of 16310 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7

Data Source

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

Last updated: Apr 27, 2026