Shenzhen Fittop Health Technology Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3012657194
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3012657194
- DUNS number
- 544301417
- Address
- 3, 6, 8/F, BLDG 3, No.7, LangFeng Road, Xinshi, Community, Dalang, Longhua District,, Shenzhen Guangdong
Frequently asked questions
How many devices does Shenzhen Fittop Health Technology Co., Ltd. have in the registry?
The registry currently lists 7 devices for Shenzhen Fittop Health Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shenzhen Fittop Health Technology Co., Ltd.'s devices?
Among its 7 most recently registered devices, Shenzhen Fittop Health Technology Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Shenzhen Fittop Health Technology Co., Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Shenzhen Fittop Health Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shenzhen Fittop Health Technology Co., Ltd. in the registry?
The most recently registered devices listed for Shenzhen Fittop Health Technology Co., Ltd. include Fittop FCM910, Fittop FCM905, Fittop FCM902 and Fittop FCM906.