Shenzhen Meik Beauty Industry Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Shenzhen Meik Beauty Industry Co., Ltd. makes
Shenzhen Meik Beauty Industry Co., Ltd. manufactures light-based devices designed for at-home hair removal, utilizing technology to target and reduce hair growth on the skin.
Their products fall under FDA Class II regulation and are listed via the 510(k) pathway in the United States. The company is based in Shenzhen, China, with regulatory submissions filed in the US market.
Catalogue
Light Based Hair Removal Device Ref K232846
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shenzhen Meik Beauty Industry Co., Ltd. have in the registry?
The registry currently lists 1 device for Shenzhen Meik Beauty Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shenzhen Meik Beauty Industry Co., Ltd.'s devices?
Among its 1 most recently registered device, Shenzhen Meik Beauty Industry Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shenzhen Meik Beauty Industry Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shenzhen Meik Beauty Industry Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shenzhen Meik Beauty Industry Co., Ltd. in the registry?
The most recently registered devices listed for Shenzhen Meik Beauty Industry Co., Ltd. include Light Based Hair Removal Device.