Data / Medical devices / Dressing, Wound, Drug / Canada
FDA-registered makers of Dressing, Wound, Drug in Canada: 5 establishments
5 establishments in Canada are registered with the FDA to make Dressing, Wound, Drug (product code FRO). 4 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
- Dressing, Wound, Drug
- Product code
- FRO
- Country
- Canada
Makers of Dressing, Wound, Drug in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Derma Sciences Canada, Inc | TORONTO Ontario, Canada | Contract manufacturer, Manufacturer | 6 | June 27, 2008 | 0 | 0 | 0 | api.fda.gov |
| Covalon Technologies Inc. | MISSISSAUGA Ontario, Canada | Complaint file establishment, Manufacturer, Specification developer | 3 | August 13, 2012 | 0 | 0 | 0 | api.fda.gov |
| Exciton Technologies Inc. | Edmonton Alberta, Canada | Manufacturer | 3 | December 6, 2018 | 0 | 0 | 0 | api.fda.gov |
| Kane Biotech Inc | Winnipeg Manitoba, Canada | Manufacturer, Specification developer | 2 | January 8, 2026 | 0 | 0 | 0 | api.fda.gov |
| Mountain Integrated Medical Devices Inc. | Edmonton Alberta, Canada | 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.