FDA applicant

Medix Medical Electronics (U.S.A.), Inc.

Mchenry, IL14 decisions1981–19860 recalls

FDA records 14 decisions for Medix Medical Electronics (U.S.A.), Inc. (Mchenry, IL) from 1981 to 1986: 14 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and BZQ (Monitor, Breathing Frequency). 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 Medix Medical Electronics (U.S.A.), Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medix Medical Electronics (U.S.A.), Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medix Medical Electronics (U.S.A.), Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medix Medical Electronics (U.S.A.), Inc.’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

Other applicant names beginning “Medix”

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

Medix Biotech, Inc. 39 Medix I.C.S.A. 6 Medix Corp. 6 Medix Biochemica 1 Medix of Florida, Inc. 1 Medix Pharmaceuticals Americas, Inc. 1

Medix Medical Electronics (U.S.A.), Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medix”