Orthosoft Inc. (d/b/a) Zimmer CAS - FDA 510(k) Cleared Devices

Orthosoft Inc. (d/b/a) Zimmer CAS has 20 FDA 510(k) cleared orthopedic devices. Based in Montreal, CA.

Latest FDA clearance: Jun 2026. Active since 2017.

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 Orthosoft Inc (D/B/A Zimmer Cas) and Orthosoft Inc. (D/B/A) Zimmer Cas). 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.