Sleepwright
Country not established
- Devices
- 1
What Sleepwright makes
Sleepwright makes medical devices such as AURADORM, which is a neuromuscular sleep device.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Auradorm (Neuromuscular Sleep) Ref K101155
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sleepwright have in the registry?
The registry currently lists 1 device for Sleepwright. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sleepwright's devices?
Among its 1 most recently registered device, Sleepwright has devices listed in FDA 510(k) (1 device).
What risk classes do Sleepwright's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sleepwright's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sleepwright in the registry?
The most recently registered devices listed for Sleepwright include AURADORM (NEUROMUSCULAR SLEEP).