Snorefree, Inc.
Country not established
- Devices
- 1
What Snorefree, Inc. makes
Snorefree, Inc. manufactures the OSAP, a device designed to address obstructive sleep apnea through oral appliance therapy, providing custom-fitted oral appliances for patients.
The OSAP is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Osap Ref K960673
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Snorefree, Inc. have in the registry?
The registry currently lists 1 device for Snorefree, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Snorefree, Inc.'s devices?
Among its 1 most recently registered device, Snorefree, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Snorefree, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Snorefree, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Snorefree, Inc. in the registry?
The most recently registered devices listed for Snorefree, Inc. include OSAP.