Guangzhou Ahead Intelligent Technology Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3019864920
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Guangzhou Ahead Intelligent Technology Co., Ltd. makes
Guangzhou Ahead Intelligent Technology Co., Ltd. manufactures light therapy systems, including models such as the M500 and L6, designed for therapeutic applications.
These devices fall under Class II regulation and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Light Therapy System (M500, L6) Ref K251042
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019864920
- Address
- Room 304, Building 4, No. 9 Shinan Second Road, Huijiang Village, Dashi Street, Panyu District, Guangzhou Guangdong
Frequently asked questions
How many devices does Guangzhou Ahead Intelligent Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Guangzhou Ahead Intelligent Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Guangzhou Ahead Intelligent Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Guangzhou Ahead Intelligent Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Guangzhou Ahead Intelligent Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Guangzhou Ahead Intelligent Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Guangzhou Ahead Intelligent Technology Co., Ltd. in the registry?
The most recently registered devices listed for Guangzhou Ahead Intelligent Technology Co., Ltd. include Light Therapy System (M500, L6).