Mvitro Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ortiv (Ortiv-Bl, Ortiv-Wh) Ref K241646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mvitro Co., Ltd. have in the registry?
The registry currently lists 1 device for Mvitro Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mvitro Co., Ltd.'s devices?
Among its 1 most recently registered device, Mvitro Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mvitro Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mvitro Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mvitro Co., Ltd. in the registry?
The most recently registered devices listed for Mvitro Co., Ltd. include ORTIV (ORTIV-BL, ORTIV-WH).