FDA applicant

Endocrine Sciences Products

Mchenry, IL2 decisions1984–19940 recalls

FDA records 2 decisions for Endocrine Sciences Products (Mchenry, IL) from 1984 to 1994: 2 510(k) clearances. Most are in product codes LCP (Assay, Glycosylated Hemoglobin) and CFL (Radioimmunoassay, Human Growth Hormone). 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, hematology panel, where it files most

How often FDA has decided Endocrine Sciences Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endocrine Sciences Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Endocrine Sciences Products’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 “Endocrine”

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

Endocrine-Metabolic Center 9 Endocrine Associates, Inc. 2

Endocrine Sciences Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Endocrine”