Krenerb, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3031464228
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3031464228
- Address
- 503 Wilson Dr, Hockessin, DE, 19707
Frequently asked questions
How many devices does KRENERB, LLC have in the registry?
The registry currently lists 2 devices for KRENERB, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list KRENERB, LLC's devices?
Among its 2 most recently registered devices, KRENERB, LLC has devices listed in FDA GUDID (2 devices).
What risk classes do KRENERB, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for KRENERB, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from KRENERB, LLC in the registry?
The most recently registered devices listed for KRENERB, LLC include FlowKeepers Gel Pads Gel Pad Envelope and FlowKeepers EP-201 Pro Bundle.