Beijing Kreate Medical Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3038550164
- Devices
- 35
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 35 devicesCompany details
- FDA FEI number
- 3038550164
- DUNS number
- 843094168
- Address
- C306, West Ring South Road #18, E-town, Beijing
Frequently asked questions
How many devices does Beijing Kreate Medical Co., Ltd. have in the registry?
The registry currently lists 35 devices for Beijing Kreate Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beijing Kreate Medical Co., Ltd.'s devices?
Among its 35 most recently registered devices, Beijing Kreate Medical Co., Ltd. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (32 devices). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from Beijing Kreate Medical Co., Ltd. in the registry?
The most recently registered devices listed for Beijing Kreate Medical Co., Ltd. include Redermax® Antibacterial Wound Matrix RDMX-14D, Redermax® Antibacterial Wound Matrix RDMX-2525, Redermax® Antibacterial Wound Matrix RDMX-5050 and Redermax® Antibacterial Wound Matrix RDMX-5075.