Data / Medical devices / Material, Tooth Shade, Resin / China
FDA-registered makers of Material, Tooth Shade, Resin in China: 8 establishments
8 establishments in China are registered with the FDA to make Material, Tooth Shade, Resin (product code EBF). 8 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Material, Tooth Shade, Resin
- Product code
- EBF
- Country
- China
Makers of Material, Tooth Shade, 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 | 4 | April 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Rizhao Huge Biomaterials Company, Ltd. | Rizhao Shandong, China | Manufacturer | 4 | December 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou Shining3d Dental Technology Co., Ltd | Hangzhou Zhejiang, China | Manufacturer | 3 | April 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Guilin Kevin Peter Technology Co., Ltd. | Guilin Guangxi, China | Manufacturer | 1 | August 31, 2026 | 0 | 0 | 0 | api.fda.gov |
| Liaoning Upcera Co.,Ltd | Benxi Liaoning, China | Manufacturer | 1 | January 12, 2017 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Piocreat 3D Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | October 15, 2024 | 0 | 0 | 0 | api.fda.gov |
| Sincera Technology (changchun) Co., Ltd | Changchun City Jilin, China | Manufacturer | 1 | March 15, 2024 | 0 | 0 | 0 | api.fda.gov |
| Sino-Dentex Co.,ltd | Changchun Jilin, China | Manufacturer | 1 | November 14, 2018 | 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.