FDA applicant

Varian Canada, Inc.

Canada L7g 2j4, CA7 decisions1991–19950 recalls

FDA records 7 decisions for Varian Canada, Inc. (Canada L7g 2j4, CA) from 1991 to 1995: 7 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and IZH (System, X-Ray, Mammographic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Varian Canada, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Varian Canada, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Varian Canada, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Varian Canada, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Varian”

FDA records each applicant name separately; these may or may not be the same firm.

Varian Medical Systems, Inc. 206 Varian Assoc., Inc. 86 Varian, Inc. 5 Varian Medical Systems, Oncology Systems 4 Varian Medical Systems, X-Ray Products-Infimed 2

Varian Canada, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Varian”