D&S Redhage
Country not established
- Devices
- 1
What D&S Redhage makes
D&S Redhage manufactures The Breathe EZ Anti-Snoring Device, a Class II medical device designed to reduce snoring by improving airway patency during sleep.
The device is regulated under FDA 510(k) clearance as a Class II product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
The Breathe Ez Anti-Snoring Device Ref K022891
510(k) 510(k)
Frequently asked questions
How many devices does D&S Redhage have in the registry?
The registry currently lists 1 device for D&S Redhage. Devices recorded under merged duplicate company entries are counted once.
Which registries list D&S Redhage's devices?
Among its 1 most recently registered device, D&S Redhage has devices listed in FDA 510(k) (1 device).
What risk classes do D&S Redhage's devices fall under?
Among its 1 most recently registered device, the classes recorded for D&S Redhage's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D&S Redhage in the registry?
The most recently registered devices listed for D&S Redhage include THE BREATHE EZ ANTI-SNORING DEVICE.