510(k) Report

FDA applicant

Jordan Neuroscience, Inc.

Redlands, CA2 decisions2005–20140 recalls

FDA records 2 decisions for Jordan Neuroscience, Inc. (Redlands, CA) from 2005 to 2014: 2 510(k) clearances. Most are in product codes OMC (Reduced- Montage Standard Electroencephalograph) and GXY (Electrode, Cutaneous). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Jordan Neuroscience, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Jordan Neuroscience, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • OMCReduced- Montage Standard Electroencephalograph1decision
  • GXYElectrode, Cutaneous1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K043009Brainet KitJordan Neuroscience, Inc. · 20051cites it

What has FDA decided for it lately?

  • K131944IEEGJordan Neuroscience, Inc. · 2014
  • K043009Brainet KitJordan Neuroscience, Inc. · 2005

All 2 as Jordan Neuroscience, Inc. →