Hans Biomed Corporation - FDA 510(k) Cleared Devices
Recent clearances: MINT MONO Sutures, 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
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hans Biomed Corporation General & Plastic Surgery ✕
4 devices
Cleared
Sep 18, 2026
MINT MONO Sutures
General & Plastic Surgery
263d
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
Jun 12, 2013
MINT
General & Plastic Surgery
138d