FDA applicant

Dura Corp., The

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Dura Corp., The (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code KCX (Epilator, High Frequency, Tweezer-Type). 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 Dura Corp., The’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dura Corp., The since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dura Corp., The’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Dura”

FDA records each applicant name separately; these may or may not be the same firm.

Dura Pharmaceuticals, Inc. 3 Dura Tap, LLC 2 Dura-Vac Products 1

Dura Corp., The

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dura”