STERIS Corporation - FDA 510(k) Cleared Devices

STERIS Corporation has 203 FDA 510(k) cleared general hospital devices. Based in Mentor, US.

Latest FDA clearance: Jun 2026. Active since 1997.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.