Tecres S.P.A. - FDA 510(k) Cleared Devices

Tecres S.P.A. has 14 FDA 510(k) cleared orthopedic devices. Based in Bethesda, US.

Latest FDA clearance: Aug 2025. Active since 2005.

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 Brauer Device Consultants, LLC and MCRA.