Data / Medical devices / Accessories, Wheelchair / Canada
FDA-registered makers of Accessories, Wheelchair in Canada: 11 establishments
11 establishments in Canada are registered with the FDA to make Accessories, Wheelchair (product code KNO). 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
- Accessories, Wheelchair
- Product code
- KNO
- Country
- Canada
Makers of Accessories, Wheelchair in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Amylior, Inc. | Vaudreuil-Dorion Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Broda LP | Kitchener Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cheelcare | Markham Ontario, Canada | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Daedalus Technologies Inc | Richmond British Columbia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Future Mobility Healthcare Inc. | MISSISSAUGA Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinova | Boisbriand Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motion Concepts LP | Vaughan Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PDG Product Design Group, Inc. | Richmond British Columbia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Power Plus Mobility Inc | Guelph Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Symmetric Designs, Ltd. | SALT SPRING ISLAND British Columbia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SYNETIK Group Inc. | Joliette Quebec, Canada | 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.