ArthroCare Corporation - FDA 510(k) Cleared Devices

ArthroCare Corporation has 36 FDA 510(k) cleared medical devices. Based in Irvine, US.

Latest FDA clearance: Mar 2026. Active since 2011. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by ArthroCare Corporation Filter by specialty or product code using the sidebar.