Dermascalp, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Dermascalp, LLC makes
Dermascal, LLC manufactures low-level laser therapy devices, specifically the DermaScalp Laser Cap, designed for hair regrowth and scalp treatment.
The company’s portfolio is classified under FDA Class II devices and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
DermaScalp Laser Cap Ref K152587
Regimes: 510(k) Registry: 510(k)DermaScalp Laser Cap Ref K173846
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermascalp, LLC have in the registry?
The registry currently lists 2 devices for Dermascalp, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermascalp, LLC's devices?
Among its 2 most recently registered devices, Dermascalp, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Dermascalp, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dermascalp, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermascalp, LLC in the registry?
The most recently registered devices listed for Dermascalp, LLC include DermaScalp Laser Cap.