Clairity, Inc.
United Statesfrom the FDA registration address FDA FEI 3042248140
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Allix5 Ref DEN240047
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 3042248140
- DUNS number
- 118193232
- Address
- 361 Newbury St Ste 402, Boston, MA, 02115
Frequently asked questions
How many devices does Clairity, Inc. have in the registry?
The registry currently lists 2 devices for Clairity, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clairity, Inc.'s devices?
Among its 2 most recently registered devices, Clairity, Inc. 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 Clairity, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clairity, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clairity, Inc. in the registry?
The most recently registered devices listed for Clairity, Inc. include Clairity Breast 10.4.5 and Allix5.