FDA applicant

Cunningham Woodland, Inc.

Mchenry, IL10 decisions1981–19830 recalls

FDA records 10 decisions for Cunningham Woodland, Inc. (Mchenry, IL) from 1981 to 1983: 10 510(k) clearances. Most are in product codes LDQ (Unnamed device) and FSM (Tray, Surgical, Instrument). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Cunningham Woodland, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cunningham Woodland, Inc.

Which product codes does it file in?

What has FDA decided for it lately?