Wettrust Korea Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Wettrust Korea Co., Ltd. makes
Wettrust Korea Co., Ltd. manufactures the wettrust D2care device, which is a Class II medical device.
The device is listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
wettrust D2care Ref K170797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wettrust Korea Co., Ltd. have in the registry?
The registry currently lists 1 device for Wettrust Korea Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wettrust Korea Co., Ltd.'s devices?
Among its 1 most recently registered device, Wettrust Korea Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wettrust Korea Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wettrust Korea Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wettrust Korea Co., Ltd. in the registry?
The most recently registered devices listed for Wettrust Korea Co., Ltd. include wettrust D2care.