Ossvis Co., Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories2
Latest Approval2024-12-05
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K242703 | LW Pre-milled Abutment | NHA | 2024-12-05 | View |
| 510(k) | K242379 | LL Implant System | DZE | 2024-11-07 | View |
| 510(k) | K233808 | LW Narrow Implant System | DZE | 2024-07-31 | View |
| 510(k) | K233167 | LW Implant System Abutment | NHA | 2024-03-25 | View |
| 510(k) | K231235 | LW UCLA Abutment | NHA | 2023-09-15 | View |
| 510(k) | K231079 | LW Retraction Cap | NHA | 2023-09-14 | View |
| 510(k) | K223924 | LW Implant System | DZE | 2023-08-08 | View |
No matching devices.