Wuhan Phomed Technology Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3026939957
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CureLight Medical Diode Laser Systems (S3-BF45) Ref K262346
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026939957
- DUNS number
- 725228743
- Address
- Room 02, 3F, Building 2, Gezhouba Sun City, No. 40 Gaoxin 4th Road, Wuhan Hubei
Frequently asked questions
How many devices does WUHAN PHOMED TECHNOLOGY CO., LTD. have in the registry?
The registry currently lists 1 device for WUHAN PHOMED TECHNOLOGY CO., LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list WUHAN PHOMED TECHNOLOGY CO., LTD.'s devices?
Among its 1 most recently registered device, WUHAN PHOMED TECHNOLOGY CO., LTD. has devices listed in FDA 510(k) (1 device).
What risk classes do WUHAN PHOMED TECHNOLOGY CO., LTD.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for WUHAN PHOMED TECHNOLOGY CO., LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from WUHAN PHOMED TECHNOLOGY CO., LTD. in the registry?
The most recently registered devices listed for WUHAN PHOMED TECHNOLOGY CO., LTD. include CureLight Medical Diode Laser Systems (S3-BF45).