Data / Medical devices / Drape, Surgical, Exempt / Canada
FDA-registered makers of Drape, Surgical, Exempt in Canada: 6 establishments
6 establishments in Canada are registered with the FDA to make Drape, Surgical, Exempt (product code PUI). 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
- Drape, Surgical, Exempt
- Product code
- PUI
- Country
- Canada
Makers of Drape, Surgical, Exempt in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arbutus Medical, Inc | Burnaby British Columbia, 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 | |
| Kent Imaging Inc | Calgary Alberta, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lac-Mac Limited | LONDON Ontario, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moleculight Inc. | TORONTO Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novadaq Technologies ULC | Burnaby British Columbia, Canada | 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.