Cgx, LLC
United Statesfrom the FDA registration address FDA FEI 3015614098
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Quick-20m Ref K203331
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015614098
- DUNS number
- 117158699
- Address
- 8445 Camino Santa Fe, San Diego, CA, 92121
- [email protected]
- Phone
- 8588649400
Frequently asked questions
How many devices does Cgx, LLC have in the registry?
The registry currently lists 2 devices for Cgx, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cgx, LLC's devices?
Among its 2 most recently registered devices, Cgx, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cgx, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cgx, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cgx, LLC in the registry?
The most recently registered devices listed for Cgx, LLC include Quick-20m SYS-0001-D and Quick-20m.