510(k) Report

FDA applicant

Corning Medical & Scientific

Mchenry, IL111 decisions1976–19880 recalls

FDA records 111 decisions for Corning Medical & Scientific (Mchenry, IL) from 1976 to 1988: 111 510(k) clearances. Most are in product codes JLW (Radioimmunoassay, Thyroid-Stimulating Hormone) and JHX (Fluorometric Method, Cpk Or Isoenzymes). 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, clinical chemistry panel, where it files most

How often FDA has decided Corning Medical & Scientific’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Corning Medical & Scientific since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Corning”

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