510(k) Report

FDA applicant

Medical Technomics, Ltd.

Mchenry, IL6 decisions1984–19850 recalls

FDA records 6 decisions for Medical Technomics, Ltd. (Mchenry, IL) from 1984 to 1985: 6 510(k) clearances. Most are in product codes JQW (Station, Pipetting And Diluting, For Clinical…) and GIO (Tube, Collection, Capillary Blood). 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 Medical Technomics, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Technomics, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Technomics, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report