Data / Medical devices / Tape And Bandage, Adhesive / Canada
FDA-registered makers of Tape And Bandage, Adhesive in Canada: 10 establishments
10 establishments in Canada are registered with the FDA to make Tape And Bandage, Adhesive (product code KGX). 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
- Tape And Bandage, Adhesive
- Product code
- KGX
- Country
- Canada
Makers of Tape And Bandage, Adhesive 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 | |
| Blistape Inc. | Edmonton Alberta, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Derma Sciences Canada, Inc | TORONTO Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heali Medical Corp | Vaughan Ontario, Canada | Exporter to the US, Foreign private label distributor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICENTIA Inc | Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kosma-Kare Canada Inc. | St-Hubert Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC) | GANANOQUE Ontario, Canada | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SDP Inc. | Saint-Laurent Quebec, Canada | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wasip Ltd. | TORONTO Ontario, Canada | Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Web-Tex, Inc. | MONTREAL, Quebec, Canada | Exporter to the US, 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.