Oneday Biotech Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-02-21
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231753 | Oneday Implant Abutment | NHA | 2024-02-21 | View |
| 510(k) | K222946 | Oneday Mini Implant System | DZE | 2023-08-23 | View |
No matching devices.