Data / Medical devices / System, X-Ray, Fluoroscopic, Image-Intensified / China
FDA-registered makers of System, X-Ray, Fluoroscopic, Image-Intensified in China: 8 establishments
8 establishments in China are registered with the FDA to make System, X-Ray, Fluoroscopic, Image-Intensified (product code JAA). 1 has 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
- System, X-Ray, Fluoroscopic, Image-Intensified
- Product code
- JAA
- Country
- China
Makers of System, X-Ray, Fluoroscopic, Image-Intensified in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ming Fai Industrial (shenzhen) Co. Ltd. | SHENZHEN Guangdong, China | Contract manufacturer, Repackager or relabeler | 1 | April 9, 1985 | 0 | 0 | 0 | api.fda.gov |
| Careray Digital Medical Technology Co., Ltd. | SuZhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Hangwei Medical Systems Co., Ltd. | Beijing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gri Medical & Electronic Technology Co., Ltd. | JIAXING Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai United Imaging Healthcare Co.,ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Shanghai, Medical Equipment Ltd. | Shanghai, China | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Shenzhen Magnetic Resonance Ltd. | SHENZHEN Guangdong, 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.