Stericycle, Inc.
United Statesfrom the FDA registration address FDA FEI 3007097064
Stericycle, Inc. is a medical device manufacturer, with 28 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 28
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 27
- FDA 510(k) 1
- Device classes
- FDA Class II 28
- Identifiers
- FDA FEI 3007097064
- DUNS 363596297
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 28 devicesCompany details
- FDA FEI number
- 3007097064
- DUNS number
- 363596297
- Address
- 2355 Waukegan Road, Bannockburn, IL, 60015
Frequently asked questions
How many devices does Stericycle, Inc. have in the registry?
The registry currently lists 28 devices for Stericycle, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stericycle, Inc.'s devices?
Among its 28 most recently registered devices, Stericycle, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (27 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Stericycle, Inc.'s devices fall under?
Among its 28 most recently registered devices, the classes recorded for Stericycle, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stericycle, Inc. in the registry?
The most recently registered devices listed for Stericycle, Inc. include Safe Returns Sharps Collection Container (UC) 101-002UC, Stericycle Reusable Sharps Container C-04/2BRX, Stericycle Reusable Sharps Container C-04RES and Stericycle Reusable Sharps Container C-04/2RES-PG.