Data / Medical devices / Alloy, Other Noble Metal / China
FDA-registered makers of Alloy, Other Noble Metal in China: 12 establishments
12 establishments in China are registered with the FDA to make Alloy, Other Noble Metal (product code EJS). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Alloy, Other Noble Metal
- Product code
- EJS
- Country
- China
Makers of Alloy, Other Noble Metal in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aidite (qinhuangdao) Technology Co., Ltd | Qinhuangdao City Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deprag High Tech Materials ( Zhengzhou ) Co.,ltd. | ZHANGZHOU Henan, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Digital Dental Depot | zhuhai Guangdong, China | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fseven Dental Technology Zhuhai Co.,ltd | ZHUHAI Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hunan Ceramaster Material Technology Co., Ltd | Changsha Hunan, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Liaoning Xinaite Technology Co.,ltd | benxi Liaoning, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qinhuangdao Audental Metal Technology Co., Ltd. | Qinhuangdao City Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shen Fu Arts Lab | Shen Zhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen HLD Dental&technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Times Dental Lab | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunrise Dental Laboratory, Ltd. | Kowloon, Hong Kong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shandong Huge Dental Material Corporation | Rizhao Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.