Techfit Digital Surgery
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K250297 | TECHFIT Patient-Specific Cranial System | October 27, 2025 |
| K242263 | TECHFIT DISRP® System | December 11, 2024 |
| K230276 | TECHFIT DISRP® System | June 23, 2023 |
| K222577 | TECHFIT Diagnostic Models | January 6, 2023 |
| K220199 | AFFINITY Proximal Tibia System | March 21, 2022 |