FDA applicant

Verite Scientific, Inc.

Mchenry, IL2 decisions1977–19770 recalls

FDA records 2 decisions for Verite Scientific, Inc. (Mchenry, IL) in 1977: 2 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and GXY (Electrode, Cutaneous). 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 Verite Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Verite Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Verite”

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

Verite 10

Verite Scientific, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Verite”