Sweet Dreams, Inc.
Country not established
- Devices
- 1
What Sweet Dreams, Inc. makes
Sweet Dreams, Inc. manufactures the Sweet Dreams Simulator, a medical training device designed for procedural practice and skill development in clinical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device and is listed in the U.S. regulatory registry.
Catalogue
Sweet Dreems Simulator Ref K860596
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sweet Dreams, Inc. have in the registry?
The registry currently lists 1 device for Sweet Dreams, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sweet Dreams, Inc.'s devices?
Among its 1 most recently registered device, Sweet Dreams, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sweet Dreams, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sweet Dreams, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sweet Dreams, Inc. in the registry?
The most recently registered devices listed for Sweet Dreams, Inc. include SWEET DREEMS SIMULATOR.