Somnowell, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Somnowell, Ltd. makes
Somnowell, Ltd. makes the Somnowell Mandibular Advancement Appliance (MAA), a dental device designed to treat snoring and obstructive sleep apnea by repositioning the lower jaw forward during sleep.
The Somnowell Mandibular Advancement Appliance 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
Somnowell Mandibular Advancement Appliance (MAA) Ref K150941
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Somnowell, Ltd. have in the registry?
The registry currently lists 1 device for Somnowell, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Somnowell, Ltd.'s devices?
Among its 1 most recently registered device, Somnowell, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Somnowell, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Somnowell, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Somnowell, Ltd. in the registry?
The most recently registered devices listed for Somnowell, Ltd. include Somnowell Mandibular Advancement Appliance (MAA).