Shenzen Magnet Technology Co., Ltd
Country not established FDA establishment FEI 3043654373
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Bone Conduction Hearing Aid (XTS-AISW-D1) Ref K261256
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043654373
- Address
- No.901, Building 9 of Zhongyuntai Industrial Park, Songbai Rd, Tangtou community, Shiyan St, Bao'an Dist, Shenzen Guangdong
Frequently asked questions
How many devices does SHENZEN MAGNET TECHNOLOGY CO.,LTD have in the registry?
The registry currently lists 6 devices for SHENZEN MAGNET TECHNOLOGY CO.,LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list SHENZEN MAGNET TECHNOLOGY CO.,LTD's devices?
Among its 6 most recently registered devices, SHENZEN MAGNET TECHNOLOGY CO.,LTD has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SHENZEN MAGNET TECHNOLOGY CO.,LTD's devices fall under?
Among its 6 most recently registered devices, the classes recorded for SHENZEN MAGNET TECHNOLOGY CO.,LTD's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from SHENZEN MAGNET TECHNOLOGY CO.,LTD in the registry?
The most recently registered devices listed for SHENZEN MAGNET TECHNOLOGY CO.,LTD include Ultroting XTS-AISW-D2, Ultroting XTS-AISW-D1, Ultroting XTS-AISW-D3 and Ultroting XTS-B06-L.