FDA applicant

Neuro Resource Group, Inc.

Plano, TX4 decisions2005–20131 recall

FDA records 4 decisions for Neuro Resource Group, Inc. (Plano, TX) from 2005 to 2013: 4 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Its devices cite 10 predicates, 2 of them its own earlier devices. 1 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 Resource Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2011

2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Neuro Resource Group, 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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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 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 1

Neuro Resource Group, 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?

What has been recalled?

Other applicant names beginning “Neuro”