FDA applicant

Vibrant Health

Beoeil, Quebec, CA3 decisions2002–20020 recalls

FDA records 3 decisions for Vibrant Health (Beoeil, Quebec, CA) in 2002: 3 510(k) clearances. All are in product code GZO (Device, Galvanic Skin Response Measurement). 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, neurology panel, where it files most

How often FDA has decided Vibrant Health’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vibrant Health since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vibrant Health’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 “Vibrant”

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

Vibrant, Ltd. 3

Vibrant Health

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vibrant”