Data / Medical devices / Wheelchair, Powered / Taiwan
FDA-registered makers of Wheelchair, Powered in Taiwan: 11 establishments
11 establishments in Taiwan are registered with the FDA to make Wheelchair, Powered (product code ITI). 10 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
- Wheelchair, Powered
- Product code
- ITI
- Country
- Taiwan
Makers of Wheelchair, Powered in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Heartway Medical Products Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 9 | June 12, 2015 | 0 | 0 | 0 | api.fda.gov |
| Merits Health Products Co., Ltd. | Taichung City, Taiwan | Manufacturer | 8 | March 18, 2022 | 0 | 0 | 0 | api.fda.gov |
| Wu's Tech Co., Ltd. | Hsin-Chu City Hsinchu(County), Taiwan | Specification developer | 4 | February 16, 2019 | 0 | 0 | 0 | api.fda.gov |
| Pihsiang Machinery MFG. Co., Ltd. | HSINCHU COUNTY Hsinchu(County), Taiwan | Manufacturer | 3 | October 7, 2014 | 0 | 0 | 0 | api.fda.gov |
| Genemax Medical Products Industry Corp. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 2 | November 12, 2004 | 0 | 0 | 0 | api.fda.gov |
| Taiwan King Strong Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 2 | December 2, 2003 | 0 | 0 | 0 | api.fda.gov |
| Chien Ti Enterprise Co., Ltd. | Taoyuan, Taiwan | Manufacturer | 1 | August 2, 2002 | 0 | 0 | 0 | api.fda.gov |
| Freerider, Corp. | Kaohsiung, Taiwan | Manufacturer | 1 | March 20, 2017 | 0 | 0 | 0 | api.fda.gov |
| Jochu Technology Co., Ltd | Hsin Chu Hsinchu(County), Taiwan | Contract manufacturer, Manufacturer | 1 | February 12, 2016 | 0 | 0 | 0 | api.fda.gov |
| Tung Keng Enterprise Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 1 | October 7, 2022 | 0 | 0 | 0 | api.fda.gov |
| Myplastics International Co., Ltd. | Tainan, 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.