FDA applicant

Devon Industries, Inc.

Mchenry, IL47 decisions1976–19963 recalls

FDA records 47 decisions for Devon Industries, Inc. (Mchenry, IL) from 1976 to 1996: 47 510(k) clearances. Most are in product codes LDQ (Unnamed device) and FMI (Needle, Hypodermic, Single Lumen). 3 recalls are 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 Devon Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Devon Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Devon Industries, Inc.’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 “Devon”

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

Devon Medical, Inc. 13 Devon Medical Products 6 Devon Medical Products (Jiangsu), Ltd. 6 Devon Safety Products, Inc. 2

Devon Industries, 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?

What has been recalled?

Other applicant names beginning “Devon”