Medical Device Manufacturer · US , Mentor , OH

STERIS Corporation - FDA 510(k) Cleared Devices

202 submissions · 200 cleared · Since 1997
202
Total
200
Cleared
2
Denied

STERIS Corporation has 200 FDA 510(k) cleared general hospital devices. Based in Mentor, US.

Latest FDA clearance: Sep 2025. 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.

FDA 510(k) cleared devices by STERIS Corporation

202 devices
1-12 of 202

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