Dermeo
Country not established
- Devices
- 1
What Dermeo makes
Dermeo manufactures LED-based phototherapy devices, including the MEDIFLASH and ESTEFLASH systems, designed for skin rejuvenation and treatment of conditions such as acne and pigmentation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mediflash And Esteflash Ref K093168
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermeo have in the registry?
The registry currently lists 1 device for Dermeo. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermeo's devices?
Among its 1 most recently registered device, Dermeo has devices listed in FDA 510(k) (1 device).
What risk classes do Dermeo's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermeo's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermeo in the registry?
The most recently registered devices listed for Dermeo include MEDIFLASH AND ESTEFLASH.