Super Grow Lasers
Country not established
- Devices
- 2
What Super Grow Lasers makes
Super Grow Lasers manufactures Class II laser devices, including the SuperGrow 272 and Ultimate 272 models, designed for medical applications requiring low-to-moderate energy output.
These devices are regulated under the FDA’s 510(k) pathway as Class II medical devices and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
SuperGrow 272, Ultimate 272 Ref K181308
Regimes: 510(k) Registry: 510(k)SuperGrow 272, Ultimate 272 Ref K172982
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Super Grow Lasers have in the registry?
The registry currently lists 2 devices for Super Grow Lasers. Devices recorded under merged duplicate company entries are counted once.
Which registries list Super Grow Lasers's devices?
Among its 2 most recently registered devices, Super Grow Lasers has devices listed in FDA 510(k) (2 devices).
What risk classes do Super Grow Lasers's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Super Grow Lasers's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Super Grow Lasers in the registry?
The most recently registered devices listed for Super Grow Lasers include SuperGrow 272, Ultimate 272.