Precision Dental Laboratories, Inc.
Country not established
- Devices
- 1
What Precision Dental Laboratories, Inc. makes
Precision Dental Laboratories, Inc. manufactures The Quiet Sleeper, a dental device designed for oral appliance therapy to address sleep-related breathing disorders.
The company’s products are regulated as Class II medical devices in the U.S. and are listed under FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
The Quiet Sleeper Ref K012142
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Dental Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Precision Dental Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Dental Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Precision Dental Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Precision Dental Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Precision Dental Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Dental Laboratories, Inc. in the registry?
The most recently registered devices listed for Precision Dental Laboratories, Inc. include THE QUIET SLEEPER.