Dental Crafters
United Statesfrom the FDA registration address FDA FEI 3004036186
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Dental Crafters makes
Dental Crafters manufactures oral snoring appliances, designed to reposition the jaw and airway to reduce snoring symptoms in patients.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ist Snoring Appliance Ref K090911
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004036186
- Address
- 1000 Corporate Drive, Marshfield, WI, 54449
Frequently asked questions
How many devices does Dental Crafters have in the registry?
The registry currently lists 1 device for Dental Crafters. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dental Crafters's devices?
Among its 1 most recently registered device, Dental Crafters has devices listed in FDA 510(k) (1 device).
What risk classes do Dental Crafters's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dental Crafters's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dental Crafters in the registry?
The most recently registered devices listed for Dental Crafters include IST SNORING APPLIANCE.