Guangzhou Beogene Biotech Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Guangzhou Beogene Biotech Co., Ltd. makes
Guangzhou Beogene Biotech Co., Ltd. manufactures dental desensitizers designed to reduce tooth sensitivity and improve patient comfort during dental procedures.
The company’s portfolio is regulated as Class II devices under FDA 510(k) clearance requirements. The dental desensitizer is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Dental Desensitizer Ref K222891
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Guangzhou Beogene Biotech Co., Ltd. have in the registry?
The registry currently lists 1 device for Guangzhou Beogene Biotech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Guangzhou Beogene Biotech Co., Ltd.'s devices?
Among its 1 most recently registered device, Guangzhou Beogene Biotech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Guangzhou Beogene Biotech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Guangzhou Beogene Biotech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Guangzhou Beogene Biotech Co., Ltd. in the registry?
The most recently registered devices listed for Guangzhou Beogene Biotech Co., Ltd. include Dental Desensitizer.