Medicrea International SA - FDA 510(k) Cleared Devices

Medicrea International SA has 25 FDA 510(k) cleared orthopedic devices. Based in Neyron, FR.

Last cleared in 2022. Active since 2015.

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

510(k) submissions have been managed by Mcra, LLC as regulatory consultant.