FDA applicant

Biomeridian, Int.

Draper, UT2 decisions2000–20060 recalls

FDA records 2 decisions for Biomeridian, Int. (Draper, UT) from 2000 to 2006: 2 510(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 Biomeridian, Int.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomeridian, Int. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Biomeridian, Int.

Which product codes does it file in?

What has FDA decided for it lately?