Somnomed Technologies Inc., Doing Business AS Remware
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- Devices
- 1
What Somnomed Technologies Inc., Doing Business AS Remware makes
Somnomed Technologies Inc. manufactures the DreamClear device, a Class II medical device designed for the treatment of obstructive sleep apnea by delivering continuous positive airway pressure (CPAP) therapy.
The DreamClear device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
DreamClear Ref K240646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Somnomed Technologies Inc., Doing Business AS Remware have in the registry?
The registry currently lists 1 device for Somnomed Technologies Inc., Doing Business AS Remware. Devices recorded under merged duplicate company entries are counted once.
Which registries list Somnomed Technologies Inc., Doing Business AS Remware's devices?
Among its 1 most recently registered device, Somnomed Technologies Inc., Doing Business AS Remware has devices listed in FDA 510(k) (1 device).
What risk classes do Somnomed Technologies Inc., Doing Business AS Remware's devices fall under?
Among its 1 most recently registered device, the classes recorded for Somnomed Technologies Inc., Doing Business AS Remware's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Somnomed Technologies Inc., Doing Business AS Remware in the registry?
The most recently registered devices listed for Somnomed Technologies Inc., Doing Business AS Remware include DreamClear.