Data / Medical devices / Stand, Infusion / Canada
FDA-registered makers of Stand, Infusion in Canada: 12 establishments
12 establishments in Canada are registered with the FDA to make Stand, Infusion (product code FOX). 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
- Stand, Infusion
- Product code
- FOX
- Country
- Canada
Makers of Stand, Infusion in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Imperial Surgical Ltd. | Lachine Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| J. Sterling Industries Ltd. | Woodbridge Ontario, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| J. Sterling Industries Ltd. | Concord Ontario, Canada | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC) | GANANOQUE Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nipro Canada Corporation | LINDSAY Ontario, Canada | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novadaq Technologies ULC | Burnaby British Columbia, Canada | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Endoscopy | Toronto Ontario, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technimount Medical Inc | Quebec, Canada | Complaint file establishment, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Traverse Rescue LLC | Oakville Ontario, Canada | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Umano Medical Inc | L Islet Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Verathon Medical (canada) ULC | Burnaby British Columbia, Canada | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Verathon Medical (canada) 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.