Jiale Health Technology Shenzhen Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3031238386
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Jiale Health Technology Shenzhen Co., Ltd. makes
Jiale Health Technology Shenzhen Co., Ltd. manufactures the Air Compression Leg Massager, model K-705.
This device is classified as Class II and is listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Air Compression Leg Massager (K-705) Ref K242140
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3031238386
- Address
- 201, Builing A, No, 17, Guangjin Road, Shapu Community, Songgang Street, Bao 'an District, Shenzhen, China, Shenzhen Guangdong
Frequently asked questions
How many devices does Jiale Health Technology Shenzhen Co., Ltd. have in the registry?
The registry currently lists 1 device for Jiale Health Technology Shenzhen Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jiale Health Technology Shenzhen Co., Ltd.'s devices?
Among its 1 most recently registered device, Jiale Health Technology Shenzhen Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jiale Health Technology Shenzhen Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jiale Health Technology Shenzhen Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jiale Health Technology Shenzhen Co., Ltd. in the registry?
The most recently registered devices listed for Jiale Health Technology Shenzhen Co., Ltd. include Air Compression Leg Massager (K-705).