Craniofacial Pain Center of Idaho
Country not established
- Devices
- 1
What Craniofacial Pain Center of Idaho makes
The company produces SILENT SLEEP, a device designed to reduce snoring and improve sleep quality for patients with craniofacial pain or obstructive sleep-related breathing disorders.
The device is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Silent Sleep Ref K082849
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Craniofacial Pain Center of Idaho have in the registry?
The registry currently lists 1 device for Craniofacial Pain Center of Idaho. Devices recorded under merged duplicate company entries are counted once.
Which registries list Craniofacial Pain Center of Idaho's devices?
Among its 1 most recently registered device, Craniofacial Pain Center of Idaho has devices listed in FDA 510(k) (1 device).
What risk classes do Craniofacial Pain Center of Idaho's devices fall under?
Among its 1 most recently registered device, the classes recorded for Craniofacial Pain Center of Idaho's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Craniofacial Pain Center of Idaho in the registry?
The most recently registered devices listed for Craniofacial Pain Center of Idaho include SILENT SLEEP.