FDA applicant

Secol Co.

Mchenry, IL18 decisions1980–19810 recalls

FDA records 18 decisions for Secol Co. (Mchenry, IL) from 1980 to 1981: 18 510(k) clearances. Most are in product codes ITG (Bandage, Cast) and KKX (Drape, Surgical, Antimicrobial). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Secol Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Secol Co.

Which product codes does it file in?

What has FDA decided for it lately?