Tigon Medical
Tigon Medical appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 21, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260921 | Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line | April 21, 2026 |
| K252596 | Tigon Medical Knotless and Dual Javelin All-Suture Anchors | December 4, 2025 |
| K242529 | Tigon Medical All-Suture Anchors (ASA) | December 20, 2024 |
| K240175 | Tigon Medical Fractures, Instability, and Reconstruction (FIRE) | October 29, 2024 |
| K220464 | Tigon Medical Gryphon Anchor Line | March 22, 2023 |
| K211049 | Tigon Medical Button System | August 4, 2021 |
| K182507 | Tigon Medical Tissue Anchors | January 21, 2019 |