Solica Corporation
CanadaFDA applicant, unverified
- Devices
- 1
What Solica Corporation makes
Solica Corporation manufactures the LightStream Low Level Laser, a Class II medical device designed for therapeutic or diagnostic low-level laser applications.
The LightStream Low Level Laser is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Lightstream Low Level Laser Ref K081166
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Solica Corporation have in the registry?
The registry currently lists 1 device for Solica Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solica Corporation's devices?
Among its 1 most recently registered device, Solica Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Solica Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Solica Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solica Corporation in the registry?
The most recently registered devices listed for Solica Corporation include LIGHTSTREAM LOW LEVEL LASER.