Data / Medical devices / Wheelchair, Mechanical / Canada
FDA-registered makers of Wheelchair, Mechanical in Canada: 6 establishments
6 establishments in Canada 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
- Canada
Makers of Wheelchair, Mechanical in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Future Mobility Healthcare Inc. | MISSISSAUGA Ontario, Canada | Manufacturer | 6 | December 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| PDG Product Design Group, Inc. | Richmond British Columbia, Canada | Manufacturer | 5 | January 17, 2007 | 0 | 0 | 0 | api.fda.gov |
| Motion Composites | St-Roch-de-lAchigan Quebec, Canada | Manufacturer | 4 | May 28, 2026 | 0 | 0 | 0 | api.fda.gov |
| Bowhead Design Corp | Calgary Alberta, Canada | Manufacturer | 1 | January 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Broda LP | Kitchener Ontario, Canada | Manufacturer | 1 | July 21, 2003 | 0 | 0 | 0 | api.fda.gov |
| Power Plus Mobility Inc | Guelph Ontario, Canada | Manufacturer | 1 | October 28, 2022 | 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.