Data / Medical devices / Lift, Patient, Non-Ac-Powered / Canada
FDA-registered makers of Lift, Patient, Non-Ac-Powered in Canada: 10 establishments
10 establishments in Canada are registered with the FDA to make Lift, Patient, Non-Ac-Powered (product code FSA). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Lift, Patient, Non-Ac-Powered
- Product code
- FSA
- Country
- Canada
Makers of Lift, Patient, Non-Ac-Powered in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Amico Clinical Solutions | Richmond Hill Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amico Mobility Solutions | Richmond Hill Ontario, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arjohuntleigh Magog, Inc. | MAGOG Quebec, Canada | Manufacturer, Specification developer | 0 | 0 | 4 | 0 | api.fda.gov | |
| Atlas Acces | Saint-Hyacinthe Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Axtion Independence Mobility Inc. | Amherst Nova Scotia, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copper House Holdings Inc | Thornton Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Handicare Canada, Ltd. | Concord Ontario, Canada | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savaria Concord Lifts Inc. | BRAMPTON Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savaria Concord Lifts, Inc. | Magog Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tollos Manufacturing | Barrie Ontario, Canada | Complaint file establishment, 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.