Uincare Corp.
South KoreaFDA applicant, unverified
- Devices
- 1
What Uincare Corp. makes
Uincare Corp. manufactures the UINCARE HOME, a medical device designed for home use, though specific clinical applications are not detailed.
The UINCARE HOME falls under FDA Class II regulation and is listed via the 510(k) pathway in the United States.
Catalogue
Uincare Home Ref K172882
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Uincare Corp. have in the registry?
The registry currently lists 1 device for Uincare Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uincare Corp.'s devices?
Among its 1 most recently registered device, Uincare Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Uincare Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Uincare Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uincare Corp. in the registry?
The most recently registered devices listed for Uincare Corp. include UINCARE HOME.