Tenon Medical, Inc.
FDA Regulatory Profile
Tenon Medical, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 8, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K260477 | CATAMARAN SI Joint Fusion System | April 8, 2026 |
| K250403 | Catamaran SI Joint Fusion System | March 21, 2025 |
| K231944 | CATAMARAN SI Joint Fusion System | August 24, 2023 |
| K180818 | Catamaran Sacroiliac Joint Fixation System (CAT SIJ Fixation System) | June 13, 2018 |