Lumenxt, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3017482216
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3017482216
- Address
- 3665 Iskagna Dr, Knoxville, TN, 37919
Frequently asked questions
How many devices does LUMENXT, LLC have in the registry?
The registry currently lists 1 device for LUMENXT, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list LUMENXT, LLC's devices?
Among its 1 most recently registered device, LUMENXT, LLC has devices listed in FDA GUDID (1 device).
What risk classes do LUMENXT, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for LUMENXT, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LUMENXT, LLC in the registry?
The most recently registered devices listed for LUMENXT, LLC include Ilio 007.101..