Data / Medical devices / System, Nuclear Magnetic Resonance Imaging / China
FDA-registered makers of System, Nuclear Magnetic Resonance Imaging in China: 11 establishments
11 establishments in China are registered with the FDA to make System, Nuclear Magnetic Resonance Imaging (product code LNH). 10 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- System, Nuclear Magnetic Resonance Imaging
- Product code
- LNH
- Country
- China
Makers of System, Nuclear Magnetic Resonance Imaging in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Siemens Shenzhen Magnetic Resonance Ltd. | SHENZHEN Guangdong, China | Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer | 49 | September 1, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ge Healthcare (tianjin) Company Limited | Tianjin, China | Manufacturer, Specification developer | 36 | August 13, 2026 | 0 | 0 | 0 | api.fda.gov |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 18 | February 5, 2026 | 0 | 1 | 0 | api.fda.gov |
| GE HEALTHCARE (CHINA) CO., LTD. - Tianjin | Tianjin, China | Specification developer | 12 | February 5, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shanghai United Imaging Healthcare Co.,ltd. | Shanghai, China | Manufacturer | 12 | September 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| MRI DIVISION, Beijing Wandong Medical Technology Co.,Ltd | Beijing, China | Manufacturer | 5 | July 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Xingaoyi Medical Equipment Co., Ltd | Yuyao Zhejiang, China | Manufacturer | 2 | August 17, 2026 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Magspin Instrument Co., Ltd | Kunshan Jiangsu, China | Exporter to the US, Manufacturer | 1 | December 22, 2015 | 0 | 0 | 0 | api.fda.gov |
| Sino Canada Health Engineering Research Institute (hefei) Ltd. (scheri) | Hefei Anhui, China | Complaint file establishment, Manufacturer | 1 | March 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen RF Tech Co., Ltd. | Shenzhen Guangdong, China | Complaint file establishment, Manufacturer | 1 | March 2, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Chenguang Medical Technologies Co, Ltd | Shanghai, China | Contract 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.