Beijing Keyi Medical Device Technology Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 4
What Beijing Keyi Medical Device Technology Co., Ltd. makes
Beijing Keyi Medical Device Technology Co., Ltd. makes orthopedic implant systems, including total knee and total hip replacement systems, spinal fixation systems, and locking plate systems.
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
KeYi Total Knee System Ref K230120
Regimes: 510(k) Registry: 510(k)KeYi Total Hip System Ref K191826
Regimes: 510(k) Registry: 510(k)KeYi Spinal Fixation System Ref K190567
Regimes: 510(k) Registry: 510(k)Locking Plate System Ref K162380
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beijing Keyi Medical Device Technology Co., Ltd. have in the registry?
The registry currently lists 4 devices for Beijing Keyi Medical Device Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beijing Keyi Medical Device Technology Co., Ltd.'s devices?
Among its 4 most recently registered devices, Beijing Keyi Medical Device Technology Co., Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Beijing Keyi Medical Device Technology Co., Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Beijing Keyi Medical Device Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beijing Keyi Medical Device Technology Co., Ltd. in the registry?
The most recently registered devices listed for Beijing Keyi Medical Device Technology Co., Ltd. include KeYi Total Knee System, KeYi Total Hip System, KeYi Spinal Fixation System and Locking Plate System.