Forth Photonics Hellas SA
Country not established
- Devices
- 1
What Forth Photonics Hellas SA makes
Forth Photonics Hellas SA manufactures the DYSIS device, a medical system designed for non-invasive skin treatments using fractional laser technology.
The DYSIS device is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dysis Ref K092433
510(k) 510(k)
Frequently asked questions
How many devices does Forth Photonics Hellas SA have in the registry?
The registry currently lists 1 device for Forth Photonics Hellas SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Forth Photonics Hellas SA's devices?
Among its 1 most recently registered device, Forth Photonics Hellas SA has devices listed in FDA 510(k) (1 device).
What risk classes do Forth Photonics Hellas SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Forth Photonics Hellas SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Forth Photonics Hellas SA in the registry?
The most recently registered devices listed for Forth Photonics Hellas SA include DYSIS.