Data / Medical devices / Crown And Bridge, Temporary, Resin / China
FDA-registered makers of Crown And Bridge, Temporary, Resin in China: 11 establishments
11 establishments in China are registered with the FDA to make Crown And Bridge, Temporary, Resin (product code EBG). 8 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
- Crown And Bridge, Temporary, Resin
- Product code
- EBG
- Country
- China
Makers of Crown And Bridge, Temporary, Resin 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 | 2 | February 16, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shandong Huge Dental Material Corporation | Rizhao Shandong, China | Manufacturer | 2 | November 3, 2020 | 0 | 0 | 0 | api.fda.gov |
| Guangzhou Heygears Imc.inc | Guangzhou Guangdong, China | Specification developer | 1 | January 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou Shining3d Dental Technology Co., Ltd | Hangzhou Zhejiang, China | Manufacturer | 1 | April 17, 2026 | 0 | 0 | 0 | api.fda.gov |
| Huliang (shanghai) Bio-Tech Co., Ltd. | Shanghai, China | Manufacturer | 1 | May 12, 2023 | 0 | 0 | 0 | api.fda.gov |
| Liaoning Upcera Co.,Ltd | Benxi Liaoning, China | Manufacturer | 1 | March 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Rizhao Huge Biomaterials Company, Ltd. | Rizhao Shandong, China | Manufacturer | 1 | June 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Yamahachi Dental Material (Changshu) Co., Ltd. | Changshu city Jiangsu, China | Manufacturer | 1 | November 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Jiangxi Heygears Innovative Material Co., Ltd | Jiujiang Jiangxi, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Piocreat 3D Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Jiahong Dental Technology Co., Ltd | Shenzhen Guangdong, 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.