Orthoselect
Also registered as Orthoselect, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3010111497
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
DIBS (Digital Indirect Bonding System) Ref K192701
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010111497
- Address
- 772 E Utah Valley Dr Ste 100, American Fork, UT, 84003
Frequently asked questions
How many devices does ORTHOSELECT have in the registry?
The registry currently lists 2 devices for ORTHOSELECT. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHOSELECT's devices?
Among its 2 most recently registered devices, ORTHOSELECT 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 ORTHOSELECT's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ORTHOSELECT's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHOSELECT in the registry?
The most recently registered devices listed for ORTHOSELECT include DIBS AI 5.X.X and DIBS (Digital Indirect Bonding System).