Cmr Naviscan Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3005945241
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3005945241
- Address
- 2720 Loker Ave W Ste O, Carlsbad, CA, 92010
Frequently asked questions
How many devices does CMR NAVISCAN CORPORATION have in the registry?
The registry currently lists 3 devices for CMR NAVISCAN CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list CMR NAVISCAN CORPORATION's devices?
Among its 3 most recently registered devices, CMR NAVISCAN CORPORATION has devices listed in FDA GUDID (3 devices).
What risk classes do CMR NAVISCAN CORPORATION's devices fall under?
Among its 3 most recently registered devices, the classes recorded for CMR NAVISCAN CORPORATION's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from CMR NAVISCAN CORPORATION in the registry?
The most recently registered devices listed for CMR NAVISCAN CORPORATION include LumaGEM MBI System 8002013, LumaGEM MBI System 22128 and LumaGEM MBI System 22129.