Hans Biomed Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
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.
FDA 510(k) cleared devices by Hans Biomed Corporation
4 devices
Cleared
Mar 07, 2023
MINT Product Family (Including MINT, MINT Lift, and MINT-I Sutures), MINT...
General & Plastic Surgery
375d
Cleared
Sep 09, 2020
MINT Product Family
General & Plastic Surgery
371d
Cleared
Feb 22, 2018
SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty
Orthopedic
268d
Cleared
Jun 12, 2013
MINT
General & Plastic Surgery
138d