Steris Corporations is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Steris Corporations - FDA 510(k) Cleared Devices
Recent clearances: BioGuard Air/Water and Suction Valves, SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid Chemical Sterilant Processing System, Celerity HP Chemical Indicator (CI)
7
Total
7
Cleared
0
Denied
Steris Corporations has 7 FDA 510(k) cleared medical devices. Based in Mentor, US.
Last cleared in 2021. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Steris Corporations Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Steris Corporations
7 devices
Cleared
Jan 08, 2021
BioGuard Air/Water and Suction Valves
Gastroenterology & Urology
28d
Cleared
Mar 22, 2019
SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid...
General Hospital
59d
Cleared
Jan 04, 2019
Celerity HP Chemical Indicator (CI)
General Hospital
38d
Cleared
Jan 03, 2019
VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological...
General Hospital
37d
Cleared
Nov 20, 2018
VERIFY All-In-One STEAM Reusable Test Pack, VERIFY All-In-One STEAM Reusable...
General Hospital
29d
Cleared
Apr 04, 2018
SYSTEM 1E Liquid Chemical Sterilant Processing System
General Hospital
56d
Cleared
Feb 09, 2018
VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological...
General Hospital
150d