Hans Biomed Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hans Biomed Corporation - FDA 510(k) Cleared Devices
Recent clearances: MINT Product Family (Including MINT, MINT Lift, and MINT-I Sutures), MINT Lift ML 1043, MINT Lift ML 1013, MINT Lift 1019, MINT Lift Mini 1014, MINT Product Family, SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty
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.
Regulatory submissions have been managed by Trisler Consulting, Emergo Global Consulting, LLC and Emergo by UL.
FDA 510(k) Regulatory Record - 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