Data / Medical devices / Implant, Endosseous, Root-Form / Taiwan
FDA-registered makers of Implant, Endosseous, Root-Form in Taiwan: 5 establishments
5 establishments in Taiwan are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 4 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
- Implant, Endosseous, Root-Form
- Product code
- DZE
- Country
- Taiwan
Makers of Implant, Endosseous, Root-Form in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alliance Global Technology Co., Ltd. | Kaohsiung, Taiwan | Manufacturer | 3 | June 2, 2016 | 0 | 0 | 0 | api.fda.gov |
| Hung Chun Bio-S Co., Ltd. | Kaohsiung City, Taiwan | Manufacturer | 2 | June 11, 2018 | 0 | 0 | 0 | api.fda.gov |
| COHO Advanced Materials Tech. Co., Ltd. | Luzhu District Taoyuan, Taiwan | Manufacturer | 1 | June 4, 2014 | 0 | 0 | 0 | api.fda.gov |
| Intai Technology Corp. Implants Business Unit | Taichung City, Taiwan | Contract manufacturer, Manufacturer | 1 | May 20, 2013 | 0 | 0 | 0 | api.fda.gov |
| Dentauspex Corporation | Douliu Yunlin, Taiwan | Contract 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.