Hans Biomed Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
8
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220549MINT Product Family (Including MINT, MINT Lift, and MINT-I Sutures), MINT Lift ML 1043, MINT Lift MLMarch 7, 2023
K192423MINT Product FamilySeptember 9, 2020
K171568SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse PuttyFebruary 22, 2018
K130191MINTJune 12, 2013