Cortigent, INC.
United Statesfrom the FDA registration address FDA establishment FEI 3004081696
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3004081696
- Address
- 27200 Tourney Road, Valencia, CA, 91355
Frequently asked questions
How many devices does Cortigent, INC. have in the registry?
The registry currently lists 7 devices for Cortigent, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cortigent, INC.'s devices?
Among its 7 most recently registered devices, Cortigent, INC. has devices listed in FDA GUDID (7 devices).
What are the newest devices from Cortigent, INC. in the registry?
The most recently registered devices listed for Cortigent, INC. include Argus II Glasses, Left Eye, Dark Lenses 012013-003, Argus II Glasses, Right Eye, Clear Lenses 012012-003, Argus II Operating Room Coil 012103-003 and Argus II Glasses - Right Eye - Dark Lenses 012011-003.