Medical Device Manufacturer · US , Mentor , OH

Steris Corparation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

Steris Corparation has 2 FDA 510(k) cleared medical devices. Based in Mentor, US.

Latest FDA clearance: Feb 2025. Active since 2022. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Steris Corparation

2 devices

1-2 of 2