The Snoremaster Co.
Country not established
- Devices
- 1
What The Snoremaster Co. makes
The Snoremaster Co. manufactures the SnoreMaster Snore Remedy, a device designed to reduce snoring by creating gentle vibrations or airflow to stimulate the soft palate and upper airway.
The SnoreMaster Snore Remedy is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Snoremaster Snore Remedy Ref K932932
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Snoremaster Co. have in the registry?
The registry currently lists 1 device for The Snoremaster Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Snoremaster Co.'s devices?
Among its 1 most recently registered device, The Snoremaster Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Snoremaster Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Snoremaster Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Snoremaster Co. in the registry?
The most recently registered devices listed for The Snoremaster Co. include SNOREMASTER SNORE REMEDY.