FDA applicant

Mediquest, Inc.

Mchenry, IL2 decisions1984–19970 recalls

FDA records 2 decisions for Mediquest, Inc. (Mchenry, IL) from 1984 to 1997: 2 510(k) clearances. All are in product code EXI (Device, Paste-On For Incontinence, Sterile). 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 Mediquest, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mediquest, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mediquest, Inc.

Which product codes does it file in?

What has FDA decided for it lately?