Prosidyan, Inc.
Prosidyan, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 22, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253147 | FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft Substitute FIBERGRAFT | October 22, 2025 |
| K251648 | GPS Advanced; GPS Advanced Cannula | June 24, 2025 |
| K241426 | GPS Advanced; 5 cc GPS Advanced Cannula | July 10, 2024 |
| K213803 | FIBERGRAFT Aeridyan Matrix Bone Graft Substitute | August 23, 2022 |
| K182670 | FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute | December 20, 2018 |
| K180080 | FIBERGRAFT BG Matrix Bone Graft Substitute | April 6, 2018 |
| K171284 | FIBERGRAFT BG Matrix Bone Graft Substitute | June 30, 2017 |
| K170306 | FIBERGRAFT BG Putty Bone Graft Substitute | May 24, 2017 |
| K151154 | FIBERGRAFT BG Morsels | November 10, 2015 |
| K143533 | FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE | March 25, 2015 |
| K141956 | FIBERGRAFT BG MORSELS | August 13, 2014 |
| K132805 | BG MORSELS | March 14, 2014 |