Wiscco Development, Inc.
Country not established
- Devices
- 1
What Wiscco Development, Inc. makes
Wiscco Development, Inc. manufactures the SKALPI 3200, a device designed for scalp stimulation or hair growth treatment, utilizing low-level laser therapy.
The SKALPI 3200 is classified as a Class I medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Skalpi 3200 Ref K946382
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wiscco Development, Inc. have in the registry?
The registry currently lists 1 device for Wiscco Development, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wiscco Development, Inc.'s devices?
Among its 1 most recently registered device, Wiscco Development, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wiscco Development, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wiscco Development, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wiscco Development, Inc. in the registry?
The most recently registered devices listed for Wiscco Development, Inc. include SKALPI 3200.