Medical Device Manufacturer · US , Philedelphia , PA

Prosidyan, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2014

Total

Cleared

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.

FDA 510(k) cleared devices by Prosidyan, Inc.

12 devices

1-12 of 12

Cleared Oct 22, 2025

FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone...

FIBERGRAFT Aeridyan Matrix Bone Graft Substitute

K213803 · MQV

Orthopedic · 260d

Cleared Dec 20, 2018

FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute

K182670 · MQV

Orthopedic · 86d

Cleared Apr 06, 2018

FIBERGRAFT BG Matrix Bone Graft Substitute

K180080 · MQV

Orthopedic · 86d

Cleared Jun 30, 2017

FIBERGRAFT BG Matrix Bone Graft Substitute

K171284 · MQV

Orthopedic · 60d

Cleared May 24, 2017

FIBERGRAFT BG Putty Bone Graft Substitute

K170306 · MQV

Orthopedic · 113d

Cleared Nov 10, 2015

FIBERGRAFT BG Morsels

K151154 · MQV

Orthopedic · 194d

Cleared Mar 25, 2015

FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE

K143533 · MQV

Orthopedic · 103d

Cleared Aug 13, 2014

FIBERGRAFT BG MORSELS

Prosidyan, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Prosidyan, Inc.

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