Devicor Medical Products, Inc. - FDA 510(k) Cleared Devices

Devicor Medical Products, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Cincinnati, US.

Latest FDA clearance: Mar 2026. Active since 2012.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.