Data / Medical devices / Electrode, Cutaneous / Taiwan
FDA-registered makers of Electrode, Cutaneous in Taiwan: 10 establishments
10 establishments in Taiwan are registered with the FDA to make Electrode, Cutaneous (product code GXY). 9 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
- Electrode, Cutaneous
- Product code
- GXY
- Country
- Taiwan
Makers of Electrode, Cutaneous in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Everyway Medical Instruments Co., Ltd. | New Taipei City, Taiwan | Manufacturer | 4 | February 28, 2018 | 0 | 0 | 0 | api.fda.gov |
| Wandy Rubber Industrial Co., Ltd | New Taipei City, Taiwan | Contract manufacturer, Manufacturer | 3 | December 20, 2013 | 0 | 0 | 0 | api.fda.gov |
| Hivox Biotek Inc. | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 2 | July 25, 2014 | 0 | 0 | 0 | api.fda.gov |
| Well-Life Healthcare Limited | Jhonghe Taipei, Taiwan | Manufacturer, Specification developer | 2 | June 1, 2021 | 0 | 0 | 0 | api.fda.gov |
| Everlife Medical Equipment Co., Ltd. | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 1 | May 13, 2005 | 0 | 0 | 0 | api.fda.gov |
| Gemore Technology Co., Ltd. | TAN SHUI New Taipei, Taiwan | Manufacturer | 1 | January 4, 2007 | 0 | 0 | 0 | api.fda.gov |
| Home Care Technology Co., Ltd. | Tainan City, Taiwan | Exporter to the US, Manufacturer | 1 | March 4, 2003 | 0 | 0 | 0 | api.fda.gov |
| Valentine Intl. Ltd. | Hsichih City, Taipei Hsien, Taiwan | Exporter to the US, Manufacturer | 1 | January 4, 2007 | 0 | 0 | 0 | api.fda.gov |
| Zmi Electronics Ltd. | Kaohsiung, Taiwan | Manufacturer | 1 | June 28, 2018 | 0 | 0 | 0 | api.fda.gov |
| Asiatic Fiber Corporation | Taoyuan County, 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.