Medos International SARL - FDA 510(k) Cleared Devices

Medos International SARL has 97 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.

Latest FDA clearance: May 2026. Active since 2010.

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 Spine, DePuy Synthes and Depuy Mitek, A Johnson and Johnson Company.