Prosidyan, Inc.
Prosidyan, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2025.
Top product codes for Prosidyan, Inc.
Recent clearances by Prosidyan, Inc.
- K253147 — FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft Substitute FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute FIBERGRAFT BG Matrix Bone Graft Substitute
- K251648 — GPS Advanced; GPS Advanced Cannula
- K241426 — GPS Advanced; 5 cc GPS Advanced Cannula
- K213803 — FIBERGRAFT Aeridyan Matrix Bone Graft Substitute
- K182670 — FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute
- K180080 — FIBERGRAFT BG Matrix Bone Graft Substitute
- K171284 — FIBERGRAFT BG Matrix Bone Graft Substitute
- K170306 — FIBERGRAFT BG Putty Bone Graft Substitute
- K151154 — FIBERGRAFT BG Morsels
- K143533 — FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE
- K141956 — FIBERGRAFT BG MORSELS
- K132805 — BG MORSELS
Data sourced from openFDA. This site is unofficial and independent of the FDA.