Luben Dental Co., Inc.
Country not established
- Devices
- 1
What Luben Dental Co., Inc. makes
Luben Dental Co., Inc. manufactures the GENTEEL dental device, designed for use in professional dental procedures.
The GENTEEL device is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway in the United States.
Catalogue
Genteel Ref K863676
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luben Dental Co., Inc. have in the registry?
The registry currently lists 1 device for Luben Dental Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luben Dental Co., Inc.'s devices?
Among its 1 most recently registered device, Luben Dental Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Luben Dental Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Luben Dental Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luben Dental Co., Inc. in the registry?
The most recently registered devices listed for Luben Dental Co., Inc. include GENTEEL.