Aurality Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3039411298
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3039411298
- Address
- 580 Herndon Pkwy., Herndon, VA, 20170
Frequently asked questions
How many devices does AURALITY INC. have in the registry?
The registry currently lists 1 device for AURALITY INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list AURALITY INC.'s devices?
Among its 1 most recently registered device, AURALITY INC. has devices listed in FDA GUDID (1 device).
What risk classes do AURALITY INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for AURALITY INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from AURALITY INC. in the registry?
The most recently registered devices listed for AURALITY INC. include Empress 3D Scanner FP-31-001.