ZuriMED Technologies AG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253867 | FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit | January 2, 2026 |
| K241219 | FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instru | December 11, 2024 |