Data / Medical devices / Coil, Magnetic Resonance, Specialty / China
FDA-registered makers of Coil, Magnetic Resonance, Specialty in China: 8 establishments
8 establishments in China are registered with the FDA to make Coil, Magnetic Resonance, Specialty (product code MOS). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Coil, Magnetic Resonance, Specialty
- Product code
- MOS
- Country
- China
Makers of Coil, Magnetic Resonance, Specialty in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen RF Tech Co., Ltd. | Shenzhen Guangdong, China | Complaint file establishment, Manufacturer | 11 | April 14, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Chenguang Medical Technologies Co, Ltd | Shanghai, China | Exporter to the US, Manufacturer | 5 | July 28, 2010 | 0 | 0 | 0 | api.fda.gov |
| Philips Healthcare (Suzhou) Co., Ltd. | Suzhou Jiangsu, China | Complaint file establishment, Manufacturer | 4 | March 20, 2026 | 0 | 0 | 0 | api.fda.gov |
| Siemens Shenzhen Magnetic Resonance Ltd. | SHENZHEN Guangdong, China | Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer | 3 | January 11, 2011 | 0 | 0 | 0 | api.fda.gov |
| Ge Healthcare (tianjin) Company Limited | Tianjin, China | Manufacturer, Specification developer | 2 | February 22, 2013 | 0 | 0 | 0 | api.fda.gov |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 1 | October 25, 2012 | 0 | 0 | 0 | api.fda.gov |
| GE HEALTHCARE (CHINA) CO., LTD. - Tianjin | Tianjin, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai United Imaging Healthcare Co.,ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.