FDA applicant

Mmi, Inc.

Southfield, MI3 decisions1984–19910 recalls

FDA records 3 decisions for Mmi, Inc. (Southfield, MI) from 1984 to 1991: 3 510(k) clearances. Most are in product codes FGD (Catheter, Retention, Barium Enema With Bag) and HFW (Clamp, Umbilical). 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 Mmi, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mmi, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mmi, Inc.

Which product codes does it file in?

What has FDA decided for it lately?