Dental Imagineers, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Dental Imagineers, LLC makes
Dental Imagineers, LLC produces oral appliances for snoring and sleep-related issues, including the SNORE-AID PLUS, SNORE-AID MAX, and SLEEPBITE devices.
These Class II devices are listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Snore-Aid Plus Ref K991449
Regimes: 510(k) Registry: 510(k)Snore-Aid Max Ref K022284
Regimes: 510(k) Registry: 510(k)Sleepbite Ref K013808
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dental Imagineers, LLC have in the registry?
The registry currently lists 3 devices for Dental Imagineers, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dental Imagineers, LLC's devices?
Among its 3 most recently registered devices, Dental Imagineers, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Dental Imagineers, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dental Imagineers, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dental Imagineers, LLC in the registry?
The most recently registered devices listed for Dental Imagineers, LLC include SNORE-AID PLUS, SNORE-AID MAX and SLEEPBITE.