Data / Medical devices / Fiber, Medical, Absorbent / Canada
FDA-registered makers of Fiber, Medical, Absorbent in Canada: 5 establishments
5 establishments in Canada are registered with the FDA to make Fiber, Medical, Absorbent (product code FRL). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Fiber, Medical, Absorbent
- Product code
- FRL
- Country
- Canada
Makers of Fiber, Medical, Absorbent in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| AMD Medicom Inc. | Pointe-Claire, Montreal Quebec, Canada | Complaint file establishment, Exporter to the US, Specification developer | 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 | |
| Hygie Canada Inc. | Drummondville Quebec, Canada | Exporter to the US, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kosma-Kare Canada Inc. | St-Hubert Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Web-Tex, Inc. | MONTREAL, Quebec, Canada | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.