FDA applicant

Immuno-Diagnostic Products, Inc.

Mchenry, IL8 decisions1980–19860 recalls

FDA records 8 decisions for Immuno-Diagnostic Products, Inc. (Mchenry, IL) from 1980 to 1986: 8 510(k) clearances. Most are in product codes JWL (Antigen, Treponema Pallidum For Fta-Abs Test) and DHN (Antinuclear Antibody, Indirect…). 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, microbiology panel, where it files most

How often FDA has decided Immuno-Diagnostic Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Immuno-Diagnostic Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Immuno-Diagnostic Products, 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 “Immuno-Diagnostic”

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-Products Industries 12 Immuno Assay Corp. 10 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-Diagnostic Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Immuno-Diagnostic”