Jiangsu Betterlife Medical Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3010197022
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Jiangsu Betterlife Medical Co., Ltd. makes
Jiangsu Betterlife Medical Co., Ltd. manufactures the TinniLogic Mobile Tinnitus Management Device, a portable solution designed for managing tinnitus symptoms through targeted sound therapy and mobile application integration.
The company’s product portfolio is regulated under Class II devices in the United States and is listed in the FDA’s 510(k) registry. The manufacturer is based in the US.
Catalogue
TinniLogic Mobile Tinnitus Management Device Ref K163094
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010197022
- Address
- 11 Sihai Rd., Jiangsu
Frequently asked questions
How many devices does Jiangsu Betterlife Medical Co., Ltd. have in the registry?
The registry currently lists 1 device for Jiangsu Betterlife Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jiangsu Betterlife Medical Co., Ltd.'s devices?
Among its 1 most recently registered device, Jiangsu Betterlife Medical Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jiangsu Betterlife Medical Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jiangsu Betterlife Medical Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jiangsu Betterlife Medical Co., Ltd. in the registry?
The most recently registered devices listed for Jiangsu Betterlife Medical Co., Ltd. include TinniLogic Mobile Tinnitus Management Device.