FDA applicant

Immuno-Products Industries

Mchenry, IL12 decisions1981–19850 recalls

FDA records 12 decisions for Immuno-Products Industries (Mchenry, IL) from 1981 to 1985: 12 510(k) clearances. Most are in product codes DHN (Antinuclear Antibody, Indirect…) and LJM (Antinuclear Antibody (Enzyme-Labeled)…). 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 Immuno-Products Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Immuno-Products Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Immuno-Products Industries’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 “Immuno-Products”

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

Immuno Concepts, Inc. 36 Immuno Nuclear Corp. 30 Immuno-Mycologics, Inc. 26 Immuno Assay Corp. 10 Immuno-Diagnostic Products, Inc. 8 Immuno Concepts, N.A., Ltd. 4 Immuno Diagnostic Center, Inc. 3 Immuno-Diagnostic Laboratories 2 Immuno-U.S., Inc. 1 Immuno Pathology Labs 1

Immuno-Products Industries

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Immuno-Products”