510(k) Report

FDA applicant

Best Medical Canada, Ltd.

Ottawa, Ontario, CA1 decision2009–20090 recalls

FDA records 1 decision for Best Medical Canada, Ltd. (Ottawa, Ontario, CA) in 2009: 1 510(k) clearance. All are in product code IYE (Accelerator, Linear, Medical). 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 Best Medical Canada, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Best Medical Canada, Ltd. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Best Medical Canada, Ltd.’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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Which product codes does it file in?

  • IYEAccelerator, Linear, Medical1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K092285Portable Dosimeter Dose Verification System, Model TD-RD-90Best Medical Canada, Ltd. · 20093cite it

What has FDA decided for it lately?

  • K092285Portable Dosimeter Dose Verification System, Model TD-RD-90Best Medical Canada, Ltd. · 2009

The one decision as Best Medical Canada, Ltd. →