FDA applicant

Mgn Medical Manufacturing, Inc.

Mchenry, IL4 decisions1981–19820 recalls

FDA records 4 decisions for Mgn Medical Manufacturing, Inc. (Mchenry, IL) from 1981 to 1982: 4 510(k) clearances. Most are in product codes BYY (Tube, Aspirating, Flexible, Connecting) and KNT (Tubes, Gastrointestinal (And Accessories)). 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 Mgn Medical Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mgn Medical Manufacturing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mgn Medical Manufacturing, Inc.

Which product codes does it file in?

What has FDA decided for it lately?