Dentool, Inc.
Country not established
- Devices
- 1
What Dentool, Inc. makes
Dentool, Inc. makes the DENTOOL device, which is a dental instrument or tool used in dental procedures.
The DENTOOL device is classified as Class I and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dentool Ref K923780
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentool, Inc. have in the registry?
The registry currently lists 1 device for Dentool, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentool, Inc.'s devices?
Among its 1 most recently registered device, Dentool, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dentool, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dentool, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dentool, Inc. in the registry?
The most recently registered devices listed for Dentool, Inc. include DENTOOL.