FDA applicant

Cns, Inc.

Eden Prairie, MN14 decisions1984–19960 recalls

FDA records 14 decisions for Cns, Inc. (Eden Prairie, MN) from 1984 to 1996: 14 510(k) clearances. Most are in product codes LWF (Dilator, Nasal) and GWS (Analyzer, Spectrum, Electroencephalogram Signal). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Cns, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cns, Inc.

Which product codes does it file in?

What has FDA decided for it lately?