Prosidyan, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prosidyan, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 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, GPS Advanced, GPS Advanced
12
Total
12
Cleared
0
Denied
Prosidyan, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Philedelphia, US.
Latest FDA clearance: Oct 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP, DePuy Synthes and Mcra, LLC.
FDA 510(k) Regulatory Record - Prosidyan, Inc.
12 devices
Cleared
Oct 22, 2025
FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone...
Orthopedic
27d
Cleared
Jun 24, 2025
GPS Advanced
Orthopedic
26d
Cleared
Jul 10, 2024
GPS Advanced
Orthopedic
51d
Cleared
Aug 23, 2022
FIBERGRAFT Aeridyan Matrix Bone Graft Substitute
Orthopedic
260d
Cleared
Dec 20, 2018
FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute
Orthopedic
86d
Cleared
Apr 06, 2018
FIBERGRAFT BG Matrix Bone Graft Substitute
Orthopedic
86d
Cleared
Jun 30, 2017
FIBERGRAFT BG Matrix Bone Graft Substitute
Orthopedic
60d
Cleared
May 24, 2017
FIBERGRAFT BG Putty Bone Graft Substitute
Orthopedic
113d
Cleared
Nov 10, 2015
FIBERGRAFT BG Morsels
Orthopedic
194d
Cleared
Mar 25, 2015
FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE
Orthopedic
103d
Cleared
Aug 13, 2014
FIBERGRAFT BG MORSELS
Orthopedic
26d
Cleared
Mar 14, 2014
BG MORSELS
Orthopedic
189d