510(k) Report

FDA applicant

Great Eastern Lumber Co., Inc.

Mchenry, IL2 decisions1978–19780 recalls

FDA records 2 decisions for Great Eastern Lumber Co., Inc. (Mchenry, IL) in 1978: 2 510(k) clearances. Most are in product codes GAD (Retractor) and IZL (System, X-Ray, Mobile). 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 Great Eastern Lumber Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Great Eastern Lumber Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Great”

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