Data / Medical devices / Stimulator, Muscle, Powered / Taiwan
FDA-registered makers of Stimulator, Muscle, Powered in Taiwan: 10 establishments
10 establishments in Taiwan are registered with the FDA to make Stimulator, Muscle, Powered (product code IPF). 6 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
- Stimulator, Muscle, Powered
- Product code
- IPF
- Country
- Taiwan
Makers of Stimulator, Muscle, Powered 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 | 3 | October 29, 2003 | 0 | 0 | 0 | api.fda.gov |
| Zmi Electronics Ltd. | Kaohsiung, Taiwan | Contract manufacturer, Manufacturer | 3 | May 2, 1995 | 0 | 0 | 0 | api.fda.gov |
| Everyway Medical Instruments Co., Ltd. | New Taipei City, Taiwan | Manufacturer | 2 | December 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| Astek Technology Ltd. | Tainan, Taiwan | Exporter to the US, Manufacturer | 1 | January 11, 2020 | 0 | 0 | 0 | api.fda.gov |
| Besmed Health Business Corporation | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 1 | November 20, 2003 | 0 | 0 | 0 | api.fda.gov |
| Everlife Medical Equipment Co., Ltd. | New Taipei City, Taiwan | Contract manufacturer, Manufacturer | 1 | August 17, 2007 | 0 | 0 | 0 | api.fda.gov |
| Domex Technology Corporation | Hsinchu Hsinchu(County), Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gemore Technology Co., Ltd. | TAN SHUI New Taipei, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Valentine Intl. Ltd. | Hsichih City, Taipei Hsien, Taiwan | Exporter to the US, 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.