FDA applicant

Neurocom International, Inc.

Clackamas, OR5 decisions1985–19950 recalls

FDA records 5 decisions for Neurocom International, Inc. (Clackamas, OR) from 1985 to 1995: 5 510(k) clearances. Most are in product codes KHX (Platform, Force-Measuring) and ETY (Tester, Auditory Impedance). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Neurocom International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neurocom International, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?