Medical Device Manufacturer · US , Brea , CA

Hans Biomed Corporation - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2013

Total

Cleared

Denied

Hans Biomed Corporation has 5 FDA 510(k) cleared medical devices. Based in Brea, US.

Latest FDA clearance: Sep 2026. Active since 2013. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Hans Biomed Corporation Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Emergo by UL, Trisler Consulting and Emergo Global Consulting, LLC.

Hans Biomed Corporation is one of 16555 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hans Biomed Corporation

5 devices

1-5 of 5

Data Source

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

Last updated: Oct 05, 2026