Data / Medical devices / Cable, Electrode / Taiwan
FDA-registered makers of Cable, Electrode in Taiwan: 5 establishments
5 establishments in Taiwan are registered with the FDA to make Cable, Electrode (product code IKD). 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
- Cable, Electrode
- Product code
- IKD
- Country
- Taiwan
Makers of Cable, Electrode in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Home Care Technology Co., Ltd. | Tainan City, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Printec H.T. Electronics Corp. | New Taipei City 235, Taiwan (R.O.C.), Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| QT Medical, INC. Taiwan Branch | New Taipei City, Taiwan | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technical Services for Electronics, Inc. | New Taipei City, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Well-Life Healthcare Limited | Jhonghe 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.