510(k) Report

FDA applicant

Clinetics Corp.

Mchenry, IL9 decisions1980–19860 recalls

FDA records 9 decisions for Clinetics Corp. (Mchenry, IL) from 1980 to 1986: 9 510(k) clearances. Most are in product codes CEP (Radioimmunoassay, Luteinizing Hormone) and CGJ (Radioimmunoassay, Follicle-Stimulating 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, clinical chemistry panel, where it files most

How often FDA has decided Clinetics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clinetics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clinetics Corp.’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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