Mz Skin
United KingdomFDA applicant, unverified
- Devices
- 1
What Mz Skin makes
Mz Skin manufactures LED-based skincare devices, including the MZ Skin LightMAX Supercharged LED Mask 2.0, designed for facial treatments such as skin rejuvenation and acne management.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry. Mz Skin operates from the United States.
Catalogue
MZ Skin LightMAX Supercharged LED Mask 2.0 Ref K213184
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mz Skin have in the registry?
The registry currently lists 1 device for Mz Skin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mz Skin's devices?
Among its 1 most recently registered device, Mz Skin has devices listed in FDA 510(k) (1 device).
What risk classes do Mz Skin's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mz Skin's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mz Skin in the registry?
The most recently registered devices listed for Mz Skin include MZ Skin LightMAX Supercharged LED Mask 2.0.