510(k) Report

FDA applicant

Bexley Trading, Inc.

Folsom, CA1 decision2002–20020 recalls

FDA records 1 decision for Bexley Trading, Inc. (Folsom, CA) in 2002: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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 Bexley Trading, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bexley Trading, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bexley Trading, 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?

  • GXYElectrode, Cutaneous1decision

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.

  • K003896Lympha Vision-ExpertBexley Trading, Inc. · 20021cites it

What has FDA decided for it lately?

  • K003896Lympha Vision-ExpertBexley Trading, Inc. · 2002

The one decision as Bexley Trading, Inc. →