Steven K. Sue
Country not established
- Devices
- 1
What Steven K. Sue makes
Steven K. Sue manufactures a nose-breathing mouthpiece designed specifically for individuals who experience heavy snoring, intended to promote nasal airflow during sleep.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Nose Breathe Mouthpiece For Heavy Snorer Ref K013687
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Steven K. Sue have in the registry?
The registry currently lists 1 device for Steven K. Sue. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steven K. Sue's devices?
Among its 1 most recently registered device, Steven K. Sue has devices listed in FDA 510(k) (1 device).
What risk classes do Steven K. Sue's devices fall under?
Among its 1 most recently registered device, the classes recorded for Steven K. Sue's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Steven K. Sue in the registry?
The most recently registered devices listed for Steven K. Sue include NOSE BREATHE MOUTHPIECE FOR HEAVY SNORER.