Keya Medical Technology Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
DEEPVESSEL Plaque Ref K260497
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 551093357
Frequently asked questions
How many devices does Keya Medical Technology Co., Ltd. have in the registry?
The registry currently lists 3 devices for Keya Medical Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keya Medical Technology Co., Ltd.'s devices?
Among its 3 most recently registered devices, Keya Medical Technology Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Keya Medical Technology Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Keya Medical Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keya Medical Technology Co., Ltd. in the registry?
The most recently registered devices listed for Keya Medical Technology Co., Ltd. include DEEPVESSEL FFR V1, DEEPVESSEL Plaque V1 and DEEPVESSEL Plaque.