FDA applicant

Exco, Inc.

Mchenry, IL20 decisions1981–19850 recalls

FDA records 20 decisions for Exco, Inc. (Mchenry, IL) from 1981 to 1985: 20 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and DQO (Catheter, Intravascular, Diagnostic). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Exco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Exco, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?