FDA applicant

Medix Corp.

Le17 6db, England, GB6 decisions1978–20040 recalls

FDA records 6 decisions for Medix Corp. (Le17 6db, England, GB) from 1978 to 2004: 6 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). No recall is linked to its devices.

FDA’s records also spell it “Medix, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Medix Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Medical Electronics (U.S.A.), Inc. 14 Medix I.C.S.A. 6 Medix Biochemica 1 Medix of Florida, Inc. 1 Medix Pharmaceuticals Americas, Inc. 1

Medix Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medix”