American Dental Laser, Inc.
Country not established
- Devices
- 1
What American Dental Laser, Inc. makes
American Dental Laser, Inc. makes dental laser devices, including single-use contact handpieces.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Dental Laser, Inc. have in the registry?
The registry currently lists 1 device for American Dental Laser, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Dental Laser, Inc.'s devices?
Among its 1 most recently registered device, American Dental Laser, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Dental Laser, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Dental Laser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Dental Laser, Inc. in the registry?
The most recently registered devices listed for American Dental Laser, Inc. include AMERICAN DENTAL LASER SINGLE USE CONTACT 320 HANDP.