FDA applicant

Virbrant Health

Beoeil, Quebec, CA1 decision2002–20020 recalls

FDA records 1 decision for Virbrant Health (Beoeil, Quebec, CA) in 2002: 1 510(k) clearance. 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 Virbrant Health’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Virbrant Health since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Virbrant Health

Which product codes does it file in?

What has FDA decided for it lately?