Medical Device Manufacturer · US , Mentor , OH

STERIS Corporation - FDA 510(k) Cleared Devices

204 submissions · 202 cleared · Since 1997
204
Total
202
Cleared
2
Denied

STERIS Corporation has 202 FDA 510(k) cleared general hospital devices. Based in Mentor, US.

Latest FDA clearance: Apr 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.

FDA 510(k) Regulatory Record - STERIS Corporation
204 devices
1-12 of 204

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