FDA applicant

Medics Instrument Corp.

Mchenry, IL4 decisions1981–19910 recalls

FDA records 4 decisions for Medics Instrument Corp. (Mchenry, IL) from 1981 to 1991: 4 510(k) clearances. Most are in product codes LDF (Electrode, Pacemaker, Temporary) and FFX (System, Gastrointestinal Motility (Electrical)). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Medics Instrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medics Instrument Corp.’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

Medics Instrument Corp.

Which product codes does it file in?

What has FDA decided for it lately?