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

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 DePuy Synthes, Hogan Lovells US LLP and Mcra, LLC.