Eventum Orthopaedics, 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 |
|---|
| K252524 | Quadsense (Quadsense and Quadsense Pro) | September 9, 2025 |
| K241298 | QUADSENSE | October 4, 2024 |