FDA applicant

Lehigh Consolidated Industries

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Lehigh Consolidated Industries (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code FRZ (Device, Patient Transfer, Powered). 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 Lehigh Consolidated Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lehigh Consolidated Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lehigh”

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

Lehigh Group 1

Lehigh Consolidated Industries

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lehigh”