Data / Medical devices / Wheelchair, Mechanical / Taiwan
FDA-registered makers of Wheelchair, Mechanical in Taiwan: 9 establishments
9 establishments in Taiwan are registered with the FDA to make Wheelchair, Mechanical (product code IOR). 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
- Wheelchair, Mechanical
- Product code
- IOR
- Country
- Taiwan
Makers of Wheelchair, Mechanical in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fa Horn Trading Incorporated Company | JIAYI COUNTY Chiayi(City), Taiwan | Manufacturer | 2 | December 9, 2005 | 0 | 0 | 0 | api.fda.gov |
| Taiwan King Strong Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 2 | November 4, 2004 | 0 | 0 | 0 | api.fda.gov |
| Chang Cheng Fa Enterprise Co., Limited | SHI-KOOU SHIANG Chiayi(County), Taiwan | Manufacturer | 1 | February 15, 2001 | 0 | 0 | 0 | api.fda.gov |
| Heartway Medical Products Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 1 | December 4, 1997 | 0 | 0 | 0 | api.fda.gov |
| Maxhealth Corp. | Xizhi District, New Taipei City, Taiwan | Exporter to the US, Manufacturer | 1 | March 1, 2007 | 0 | 0 | 0 | api.fda.gov |
| Wu Ho Medical Instruments MFG. Co. Ltd. | Taipei Hsien, Taiwan, (China), Taiwan | Manufacturer | 1 | October 9, 1997 | 0 | 0 | 0 | api.fda.gov |
| Genemax Medical Products Industry Corp. | Taichung City, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rong Shin Industrial Co., Ltd. | Tainan City, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shin-I Medical Manufacturing Co. Ltd. | Taoyuan, 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.