Hans Biomed Corporation
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2023-03-07
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220549 | 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 | NEW | 2023-03-07 | View |
| 510(k) | K192423 | MINT Product Family | NEW | 2020-09-09 | View |
| 510(k) | K171568 | SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty | MQV | 2018-02-22 | View |
No matching devices.