FDA applicant

Verathon Medical (Canada) Ulc

Burnaby, CA6 decisions2019–20260 recalls

FDA records 6 decisions for Verathon Medical (Canada) Ulc (Burnaby, CA) from 2019 to 2026: 6 510(k) clearances. Most are in product codes EOQ (Bronchoscope (Flexible Or Rigid)) and FAJ (Cystoscope And Accessories, Flexible/Rigid). Since 2016 its 510(k)s took a median of 37 days from receipt to decision, against 147 for FDA’s reviews in the same codes and years. Its devices cite 10 predicates, 8 of them its own earlier devices. 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, ear, nose and throat panel, where it files most

How often FDA has decided Verathon Medical (Canada) Ulc’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2019high 2 (2019) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Verathon Medical (Canada) Ulc by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Verathon Medical (Canada) Ulc’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 “Verathon”

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

Verathon Incorporated 5

Verathon Medical (Canada) Ulc

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Verathon”