Data / Medical devices / Additively Manufactured, Preformed, Resin Denture Tooth / China
FDA-registered makers of Additively Manufactured, Preformed, Resin Denture Tooth in China: 11 establishments
11 establishments in China are registered with the FDA to make Additively Manufactured, Preformed, Resin Denture Tooth (product code PZY). 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
- Additively Manufactured, Preformed, Resin Denture Tooth
- Product code
- PZY
- Country
- China
Makers of Additively Manufactured, Preformed, Resin Denture Tooth 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 | |
| Guangzhou Heygears Imc.inc | Guangzhou Guangdong, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hangzhou Shining3d Dental Technology Co., Ltd | Hangzhou Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangxi Heygears Innovative Material Co., Ltd | Jiujiang Jiangxi, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jinyuan Medical Equipment(tianjin)co.,ltd | Tianjin, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rite Smile Labs | Shenzhenzs Inner Mongolia, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Riton 3D Technology Co., Ltd | Guangzhou Guangdong, China | 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 Yongchanghe Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Laixin 3D Technology Co.,ltd | Suzhou Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xiamen Antinsky Industry Co., Ltd | Xiamen Fujian, China | Exporter to the US, 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.