Hans Biomed Corporation - FDA 510(k) Cleared Devices

Hans Biomed Corporation has 4 FDA 510(k) cleared medical devices. Based in Brea, US.

Last cleared in 2023. 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.

510(k) submissions have been managed by Emergo by UL as regulatory consultant.