FDA Device Entity Profile: STERIS

Known Identifiers & Locations

FEI Numbers 1526531, 1923569, 3006554912

Owner Operator Numbers 10091086

Locations Covered CLEVELAND, OH, US; Saint Louis, MO, US; Wurmlingen Baden-Wurttemberg, DE

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1526531	STERIS Corporation	CLEVELAND, OH, US	Repack or Relabel Medical Device	View Details
1923569	STERIS Corporation	Saint Louis, MO, US	Manufacture Medical Device	View Details
3006554912	STERIS Deutschland GmBh	Wurmlingen Baden-Wurttemberg, DE	Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device	View Details

510(k) Premarket Notifications (1)

Submission #	Device Name	Decision Date	Decision Description	Action
K242773	Electro Lube NXT	2025-04-15	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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