American Sleep Dentistry
United Statesfrom the FDA registration address FDA establishment FEI 3008313791
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What American Sleep Dentistry makes
American Sleep Dentistry makes ASD Oral Appliances, which are dental devices used for sleep-related conditions.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
ASD Oral Appliances Ref K163580
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008313791
- Address
- 1289 S Interstate Dr, Cedar City, UT, 84720
Frequently asked questions
How many devices does AMERICAN SLEEP DENTISTRY have in the registry?
The registry currently lists 1 device for AMERICAN SLEEP DENTISTRY. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMERICAN SLEEP DENTISTRY's devices?
Among its 1 most recently registered device, AMERICAN SLEEP DENTISTRY has devices listed in FDA 510(k) (1 device).
What risk classes do AMERICAN SLEEP DENTISTRY's devices fall under?
Among its 1 most recently registered device, the classes recorded for AMERICAN SLEEP DENTISTRY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AMERICAN SLEEP DENTISTRY in the registry?
The most recently registered devices listed for AMERICAN SLEEP DENTISTRY include ASD Oral Appliances.