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
FDA 510(k) Regulatory Record - Hans Biomed Corporation Orthopedic ✕
1 devices