Pearl Digital, Inc.
Country not established
- Devices
- 1
What Pearl Digital, Inc. makes
Pearl Digital, Inc. produces the Pearl Clear Aligner, which is a dental aligner device used for orthodontic treatment.
The Pearl Clear Aligner is classified as a Class II medical device and is listed in the FDA 510(k) registry. Pearl Digital, Inc. is based in the US.
Catalogue
Pearl Clear Aligner Ref K242715
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pearl Digital, Inc. have in the registry?
The registry currently lists 1 device for Pearl Digital, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pearl Digital, Inc.'s devices?
Among its 1 most recently registered device, Pearl Digital, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pearl Digital, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pearl Digital, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pearl Digital, Inc. in the registry?
The most recently registered devices listed for Pearl Digital, Inc. include Pearl Clear Aligner.