FDA applicant

M.B. Industries, Inc.

Granite City, IL3 decisions1996–19970 recalls

FDA records 3 decisions for M.B. Industries, Inc. (Granite City, IL) from 1996 to 1997: 3 510(k) clearances. All are in product code MPA (Endoilluminator). Its devices cite 5 predicates, 2 of them its own earlier devices. 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, gastroenterology and urology panel, where it files most

How often FDA has decided M.B. Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for M.B. Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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M.B. Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?