FDA applicant

The Electrode Store, Inc.

Seattle, WA6 decisions1995–20090 recalls

FDA records 6 decisions for The Electrode Store, Inc. (Seattle, WA) from 1995 to 2009: 6 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and GXZ (Electrode, Needle). 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 The Electrode Store, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Electrode Store, 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

Other applicant names beginning “The”

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

Electrode Market Co., Ltd. 1 Electrode Arrays 1

The Electrode Store, Inc.

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 “The”