Medusa (Guangxi)Medical Devices Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Medusa (Guangxi)Medical Devices Co., Ltd. makes
Medusa (Guangxi) Medical Devices Co., Ltd. manufactures an Intense Pulsed Light (IPL) Treatment Device, designed for controlled light-based skin treatments.
The IPL Treatment Device (MDSQMC-01) is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway in the United States.
Catalogue
IPL Treatment Device (MDSQMC-01) Ref K243123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medusa (Guangxi)Medical Devices Co., Ltd. have in the registry?
The registry currently lists 1 device for Medusa (Guangxi)Medical Devices Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medusa (Guangxi)Medical Devices Co., Ltd.'s devices?
Among its 1 most recently registered device, Medusa (Guangxi)Medical Devices Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medusa (Guangxi)Medical Devices Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medusa (Guangxi)Medical Devices Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medusa (Guangxi)Medical Devices Co., Ltd. in the registry?
The most recently registered devices listed for Medusa (Guangxi)Medical Devices Co., Ltd. include IPL Treatment Device (MDSQMC-01).