ASTUTE IMAGING Inc
United Statesfrom the FDA registration address FDA establishment FEI 3021625328
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3021625328
- Address
- 53 South Main Street, Hanover, NH, 03755
Frequently asked questions
How many devices does ASTUTE IMAGING Inc have in the registry?
The registry currently lists 1 device for ASTUTE IMAGING Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list ASTUTE IMAGING Inc's devices?
Among its 1 most recently registered device, ASTUTE IMAGING Inc has devices listed in FDA GUDID (1 device).
What risk classes do ASTUTE IMAGING Inc's devices fall under?
Among its 1 most recently registered device, the classes recorded for ASTUTE IMAGING Inc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ASTUTE IMAGING Inc in the registry?
The most recently registered devices listed for ASTUTE IMAGING Inc include Preview® Treatment Planning Software 10.0.0.