Data / Medical devices / China / Shenzen Magnet Technology Co.,ltd
Shenzen Magnet Technology Co.,ltd: FDA-registered device maker in Shenzen Guangdong, China, 1 510(k) clearance
Shenzen Magnet Technology Co.,ltd is registered with the FDA (registration 3043654373) in Shenzen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 11, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3043654373
- Address
- No.901, Building 9 of Zhongyuntai Industrial Park, Songbai Rd, Tangtou community, Shiyan St, Bao'an Dist, Shenzen Guangdong, China, 518100
- Owner or operator
- Shenzen Magnet Technology Co.,Ltd (10095028)
- Roles
- Manufacturer
- First device listed
- January 15, 2026
- Registered through
- 2026
- Brand names listed
- Air conduction hearing aid (Model: XTS-B06-L, XTS-B06-M), Brand: Ultroting, Bone Conduction Hearing Aid (Models: XTS-AISW-D1, XTS-AISW-D2, XTS-AISW-D3)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hearing Aid, Air-Conduction, Over The Counter | QUF | 1 | Manufacturer | accessdata.fda.gov |
| Hearing Aid, Bone Conduction | LXB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 11, 2026 | K261256 | Bone Conduction Hearing Aid (XTS-AISW-D1, XTS-AISW-D2, XTS-AISW-D3) | LXB | Substantially Equivalent | Shenzhen Magnet Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Hearing Aid, Bone Conduction
- All makers of Hearing Aid, Air-Conduction, Over The Counter
Updated June 11, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.