TriMed, Inc. - FDA 510(k) Cleared Devices

TriMed, Inc. has 35 FDA 510(k) cleared orthopedic devices. Based in Saugus, US.

Latest FDA clearance: Jan 2026. 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.

510(k) submissions have been managed by Tech2med, LLC as regulatory consultant. 3 submissions have an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.