FDA applicant

Neurosoft, Inc.

El Paso, TX7 decisions2000–20220 recalls

FDA records 7 decisions for Neurosoft, Inc. (El Paso, TX) from 2000 to 2022: 7 510(k) clearances. Most are in product codes OLX (Source Localization Software For…) and OLT (Non-Normalizing Quantitative…). Its devices cite 7 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Neurosoft , Ltd.”.

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 Neurosoft, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Neurosoft, 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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Neurosoft, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?