Snorex, Inc.
Country not established
- Devices
- 1
What Snorex, Inc. makes
Snorex, Inc. makes the SNOR-X MOUTH GUARD, a device designed to address snoring by repositioning the jaw or tongue during sleep.
The SNOR-X MOUTH GUARD is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Snor-X Mouth Guard Ref K954324
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Snorex, Inc. have in the registry?
The registry currently lists 1 device for Snorex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Snorex, Inc.'s devices?
Among its 1 most recently registered device, Snorex, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Snorex, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Snorex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Snorex, Inc. in the registry?
The most recently registered devices listed for Snorex, Inc. include SNOR-X MOUTH GUARD.