Company · US
Techfit Digital Surgery, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2025. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 27, 2025 | K250297 | TECHFIT Patient-Specific Cranial System Techfit Digital Surgery, Inc. | GWO |
| Dec 11, 2024 | K242263 | TECHFIT DISRP® System Techfit Digital Surgery, Inc. | DZJ |
| Jun 23, 2023 | K230276 | TECHFIT DISRP® System Techfit Digital Surgery | DZJ |
| Jan 6, 2023 | K222577 | TECHFIT Diagnostic Models Techfit Digital Surgery, Inc. | LLZ |
| Mar 21, 2022 | K220199 | AFFINITY Proximal Tibia System Techfit Digital Surgery, Inc. | HRS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||