Fovia, Inc.
Country not established FDA FEI 3036471119
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Fovia, Inc. makes
Fovia, Inc. manufactures the aiCockpit AI Viewer, a device designed for analyzing and visualizing data in aviation cockpit environments using artificial intelligence.
The aiCockpit AI Viewer is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
aiCockpit AI Viewer Ref K241546
510(k) 510(k)
Company details
- FDA FEI number
- 3036471119
- Address
- 907 Sir Francis Drake Blvd, Kentfield, CA, 94904
Frequently asked questions
How many devices does Fovia, Inc. have in the registry?
The registry currently lists 1 device for Fovia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fovia, Inc.'s devices?
Among its 1 most recently registered device, Fovia, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fovia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fovia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fovia, Inc. in the registry?
The most recently registered devices listed for Fovia, Inc. include aiCockpit AI Viewer.