Data / Medical devices / System, X-Ray, Extraoral Source, Digital / China
FDA-registered makers of System, X-Ray, Extraoral Source, Digital in China: 9 establishments
9 establishments in China are registered with the FDA to make System, X-Ray, Extraoral Source, Digital (product code MUH). 7 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
- System, X-Ray, Extraoral Source, Digital
- Product code
- MUH
- Country
- China
Makers of System, X-Ray, Extraoral Source, Digital in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| iRay Group | Shanghai, China | Complaint file establishment, Manufacturer, Specification developer | 3 | October 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Guilin Woodpecker Medical Instrument Co., Ltd | GUILIN CITY Guangxi, China | Manufacturer | 2 | October 7, 2021 | 0 | 0 | 0 | api.fda.gov |
| Changzhou Sifary Medical Technology Co., Ltd. | Changzhou Jiangsu, China | Manufacturer | 1 | March 11, 2022 | 0 | 0 | 0 | api.fda.gov |
| Fussen Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | December 5, 2019 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Dynamic Medical Technology Co., Ltd | Suzhou Jiangsu, China | Exporter to the US, Manufacturer | 1 | December 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Handy Medical Equipment Co., Ltd. | Shanghai, China | Manufacturer | 1 | June 22, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Xpectvision Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | February 17, 2022 | 0 | 0 | 0 | api.fda.gov |
| Carestream Healthcare International Company, Ltd | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| iRay Imaging Technology Taicang Limited | Taicang Jiangsu, 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.