Steribite, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3009662229
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3009662229
- Address
- 1877 Eagle Pass, Wooster, OH, 44691
Frequently asked questions
How many devices does Steribite, LLC have in the registry?
The registry currently lists 9 devices for Steribite, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steribite, LLC's devices?
Among its 9 most recently registered devices, Steribite, LLC has devices listed in FDA GUDID (9 devices).
What risk classes do Steribite, LLC's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Steribite, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Steribite, LLC in the registry?
The most recently registered devices listed for Steribite, LLC include Steribite SB70852-1, Steribite SB70851-1, Steribite SB70855-1 and Steribite SB70854-1.