510(k) Report

FDA applicant

Medcare Products

Mchenry, IL20 decisions1981–19840 recalls

FDA records 20 decisions for Medcare Products (Mchenry, IL) from 1981 to 1984: 20 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) and KDC (Instrument, Surgical, Disposable). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Medcare Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Medcare”

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