Medos International SARL - FDA 510(k) Cleared Devices

Medos International SARL has 96 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.

Latest FDA clearance: Mar 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 Spine and Cerenovus.