Data / Medical devices / Accessories, Implant, Dental, Endosseous / Taiwan
FDA-registered makers of Accessories, Implant, Dental, Endosseous in Taiwan: 10 establishments
10 establishments in Taiwan are registered with the FDA to make Accessories, Implant, Dental, Endosseous (product code NDP). 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
- Accessories, Implant, Dental, Endosseous
- Product code
- NDP
- Country
- Taiwan
Makers of Accessories, Implant, Dental, Endosseous 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 | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apply Labwork Inc. | Taoyuan City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bomei Co., Ltd. | Taoyuan City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| COHO Advanced Materials Tech. Co., Ltd. | Luzhu District Taoyuan, Taiwan | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentauspex Corporation | Douliu Yunlin, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Enlighten Materials Co., Ltd. | Taipei City, Taiwan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hung Chun Bio-S Co., Ltd. | Kaohsiung City, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intai Technology Corp. Implants Business Unit | Taichung City, Taiwan | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microware Precision Co., Ltd. | Taichung, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sentronic International Corp. | Taipei, Taiwan | 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.