Prosidyan, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFTOctober 22, 2025
K251648GPS Advanced; GPS Advanced CannulaJune 24, 2025
K241426GPS Advanced; 5 cc GPS Advanced CannulaJuly 10, 2024
K213803FIBERGRAFT Aeridyan Matrix Bone Graft SubstituteAugust 23, 2022
K182670FIBERGRAFT AERIDYAN Matrix Bone Graft SubstituteDecember 20, 2018
K180080FIBERGRAFT BG Matrix Bone Graft SubstituteApril 6, 2018
K171284FIBERGRAFT BG Matrix Bone Graft SubstituteJune 30, 2017
K170306FIBERGRAFT BG Putty Bone Graft SubstituteMay 24, 2017
K151154FIBERGRAFT BG MorselsNovember 10, 2015
K143533FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTEMarch 25, 2015
K141956FIBERGRAFT BG MORSELSAugust 13, 2014
K132805BG MORSELSMarch 14, 2014