Nightware, Inc.
Country not established
- Devices
- 2
What Nightware, Inc. makes
Nightware, Inc. develops software designed to interpret and analyze sleep disorder data for patient use, including tools that monitor and respond to sleep-related conditions. The NightWare system integrates with mobile devices like the Apple iPhone and Apple Watch, using companion accessories such as charging cables for connectivity. It is intended to provide insights and interventions for individuals experiencing sleep disturbances.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. Nightware, Inc. is based in the United States.
Catalogue
- Registry: GUDID
NightWare Kit, Apple iPhone, Apple Watch, Apple iPhone Charging Cable, Apple Watch Charging Cable Ref DEN200033
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Nightware, Inc. have in the registry?
The registry currently lists 2 devices for Nightware, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nightware, Inc.'s devices?
Among its 2 most recently registered devices, Nightware, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Nightware, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nightware, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nightware, Inc. in the registry?
The most recently registered devices listed for Nightware, Inc. include NightWare 100001 and NightWare Kit, Apple iPhone, Apple Watch, Apple iPhone Charging Cable, Apple Watch Charging Cable.