Avara Software
Country not established FDA FEI 3047378919
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
Avara Viewer Ref K262120
510(k) 510(k)
Company details
- FDA FEI number
- 3047378919
- Address
- 5015 4th St N, St Petersburg, FL, 33703
Frequently asked questions
How many devices does Avara Software have in the registry?
The registry currently lists 2 devices for Avara Software. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avara Software's devices?
Among its 2 most recently registered devices, Avara Software 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 Avara Software's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Avara Software's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avara Software in the registry?
The most recently registered devices listed for Avara Software include Avara Viewer 1.0.0 and Avara Viewer.