FDA applicant

Neurovision Medical Product, Inc.

Ventura, CA1 decision2017–20170 recalls

FDA records 1 decision for Neurovision Medical Product, Inc. (Ventura, CA) in 2017: 1 510(k) clearance. All are in product code GWF (Stimulator, Electrical, Evoked Response). 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 Neurovision Medical Product, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Neurovision Medical Product, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Neurovision”

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

Neurovision Medical Products, Inc. 9 Neurovision, Inc. 1 Neurovision Imaging, LLC 1

Neurovision Medical Product, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Neurovision”