United States Dental Laser, Inc.
Country not established
- Devices
- 1
What United States Dental Laser, Inc. makes
United States Dental Laser, Inc. manufactures the Model SELECT 1000 Frequency Doubled Nd:YAG Laser System, a dental laser designed for precision procedures in oral healthcare.
This device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does United States Dental Laser, Inc. have in the registry?
The registry currently lists 1 device for United States Dental Laser, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list United States Dental Laser, Inc.'s devices?
Among its 1 most recently registered device, United States Dental Laser, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do United States Dental Laser, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for United States Dental Laser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from United States Dental Laser, Inc. in the registry?
The most recently registered devices listed for United States Dental Laser, Inc. include USDL MODEL SELECT 1000 FREQUENCY DOUBLED ND:YAG LASER SYSTEM.