Oneday Biotech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K231753 | Oneday Implant Abutment | February 21, 2024 |
| K222946 | Oneday Mini Implant System | August 23, 2023 |