Slumber Research, Inc.
Country not established
- Devices
- 1
What Slumber Research, Inc. makes
Slumber Research, Inc. manufactures the SILENTSLEEP device, which appears to be a Class I medical device designed for sleep-related applications, likely targeting noise reduction or sleep environment enhancement.
The SILENTSLEEP device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Silentsleep Ref K801927
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Slumber Research, Inc. have in the registry?
The registry currently lists 1 device for Slumber Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Slumber Research, Inc.'s devices?
Among its 1 most recently registered device, Slumber Research, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Slumber Research, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Slumber Research, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Slumber Research, Inc. in the registry?
The most recently registered devices listed for Slumber Research, Inc. include SILENTSLEEP.