510(k) Report

FDA applicant

Medicare Industries, Inc.

Mchenry, IL7 decisions1978–19890 recalls

FDA records 7 decisions for Medicare Industries, Inc. (Mchenry, IL) from 1978 to 1989: 7 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and LYY (Latex Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Medicare Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medicare Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medicare Industries, Inc.’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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