Data / Medical devices / Cover, Mattress (Medical Purposes) / Canada
FDA-registered makers of Cover, Mattress (Medical Purposes) in Canada: 8 establishments
8 establishments in Canada are registered with the FDA to make Cover, Mattress (Medical Purposes) (product code FMW). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Cover, Mattress (Medical Purposes)
- Product code
- FMW
- Country
- Canada
Makers of Cover, Mattress (Medical Purposes) in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 2712218 Ontario Inc | Concord Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| 5 Minds Mobility | Oshawa Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| AMD Medicom Inc. | Pointe-Claire, Montreal Quebec, Canada | Complaint file establishment, Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essity Canada Inc. | DRUMMONDVILLE Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| George Courey Inc | Montreal Quebec, Canada | Complaint file establishment, Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mip, Inc. | ANJOU Quebec, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtrica Solutions Ltd | Surrey British Columbia, Canada | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surface Medical, Inc. | Calgary Alberta, Canada | Specification developer | 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.