FDA applicant

Neuro Diagnostic Devices

Trevose, PA1 decision2008–20080 recalls

FDA records 1 decision for Neuro Diagnostic Devices (Trevose, PA) in 2008: 1 510(k) clearance. All are in product code JXG (Shunt, Central Nervous System And Components). 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 Neuro Diagnostic Devices’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Neuro Diagnostic Devices by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Neuro Diagnostic Devices’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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Other applicant names beginning “Neuro”

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

Neuro Navigational Corp. 23 Neuro Supplies, Inc. 5 Neuro Technology 5 Neuro Kinetics, Inc. 4 Neuro Resource Group, Inc. 4 Neuro Therm, Inc. 3 Neuro Scan Labs 3 Neuro Vasx, Inc. 2 Neuro-Biometrix, Inc. 2 Neuro-Diagnostic Assoc. 2 Neuro Event Labs OY 1 Neuro-Fitness, LLC 1

Neuro Diagnostic Devices

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?

Other applicant names beginning “Neuro”