FDA applicant

Cherne Industries, Inc.

Minneapolis, MN3 decisions1985–19860 recalls

FDA records 3 decisions for Cherne Industries, Inc. (Minneapolis, MN) from 1985 to 1986: 3 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and LGX (Table, Examination, Medical, 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, cardiovascular panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Cherne Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?