Gowoonsesang Cosmetics Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 2
What Gowoonsesang Cosmetics Co., Ltd. makes
Gowoonsesang Cosmetics Co., Ltd. makes the AGNES device and a series of GA-series devices including GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, and GA-F1A.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Agnes Ref K160469
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gowoonsesang Cosmetics Co., Ltd. have in the registry?
The registry currently lists 2 devices for Gowoonsesang Cosmetics Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gowoonsesang Cosmetics Co., Ltd.'s devices?
Among its 2 most recently registered devices, Gowoonsesang Cosmetics Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gowoonsesang Cosmetics Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gowoonsesang Cosmetics Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gowoonsesang Cosmetics Co., Ltd. in the registry?
The most recently registered devices listed for Gowoonsesang Cosmetics Co., Ltd. include AGNES and GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A.