Axcesor LLC
United Statesfrom the FDA registration address FDA establishment FEI 3003007822
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3003007822
- Address
- W134N5345 Campbell Drive, Menomonee Falls, WI, 53051
Frequently asked questions
How many devices does AXCESOR LLC have in the registry?
The registry currently lists 1 device for AXCESOR LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list AXCESOR LLC's devices?
Among its 1 most recently registered device, AXCESOR LLC has devices listed in FDA GUDID (1 device).
What risk classes do AXCESOR LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for AXCESOR LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AXCESOR LLC in the registry?
The most recently registered devices listed for AXCESOR LLC include Gentle Vac 17420.