FDA applicant

Ventrex Laboratories, Inc.

Mchenry, IL82 decisions1979–19920 recalls

FDA records 82 decisions for Ventrex Laboratories, Inc. (Mchenry, IL) from 1979 to 1992: 82 510(k) clearances. Most are in product codes DHB (System, Test, Radioallergosorbent (Rast)…) and DGC (Ige, Antigen, Antiserum, Control). 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, immunology panel, where it files most

How often FDA has decided Ventrex Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ventrex Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ventrex Laboratories, 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 “Ventrex”

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

Ventrex, Inc. 6

Ventrex Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Ventrex”