FDA applicant

Veratex Corp.

Mchenry, IL3 decisions1980–19830 recalls

FDA records 3 decisions for Veratex Corp. (Mchenry, IL) from 1980 to 1983: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and EFN (Cotton, Roll). 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 Veratex Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Veratex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Veratex Corp.

Which product codes does it file in?

What has FDA decided for it lately?