Sleep Renewal, Inc.
Country not established
- Devices
- 1
What Sleep Renewal, Inc. makes
Sleep Renewal, Inc. manufactures The Equalizer Airway Device, a medical device designed to manage obstructive sleep apnea by maintaining an open airway during sleep.
The device is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
The Equalizer Airway Device Ref K870501
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sleep Renewal, Inc. have in the registry?
The registry currently lists 1 device for Sleep Renewal, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sleep Renewal, Inc.'s devices?
Among its 1 most recently registered device, Sleep Renewal, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sleep Renewal, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sleep Renewal, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sleep Renewal, Inc. in the registry?
The most recently registered devices listed for Sleep Renewal, Inc. include THE EQUALIZER AIRWAY DEVICE.