Nuprodx, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3026952403
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3026952403
- Address
- 40380 Brickyard Drive, Madera, CA, 93636
Frequently asked questions
How many devices does NUPRODX, INC. have in the registry?
The registry currently lists 1 device for NUPRODX, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list NUPRODX, INC.'s devices?
Among its 1 most recently registered device, NUPRODX, INC. has devices listed in FDA GUDID (1 device).
What risk classes do NUPRODX, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for NUPRODX, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from NUPRODX, INC. in the registry?
The most recently registered devices listed for NUPRODX, INC. include Multichair MC.