Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list The Electrode Store, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 14, 2009: SENSORY NERVE ELECTRODES-TWO FINGER RINGS, STIMULATOR PROBE ELECTRODES-FACIAL, MONO, BI-….
| Aug 14, 2009 | SENSORY NERVE ELECTRODES-TWO FINGER RINGS, STIMULATOR PROBE ELECTRODES-FACIAL, MONO, BI- & TRIPOLAR NERVE STIMULATORSK083758 · GXY | 510(k) clearances |
| Aug 13, 2002 | SURFACE ELECTRODE FOR ELECTROENCEPHALOGRAPHYK022197 · GXY | 510(k) clearances |
| Jul 19, 2002 | SUBDERMAL NEEDLE ELECTRODE FOR ELECTROENCEPHALOGRAPHY, MODELS PRO-E12SAF AND DEN-12SAFK020910 · GXZ | 510(k) clearances |
| May 10, 2002 | THE ELECTRODE STORE SURFACE (CUTANEOUS) ELECTRODE FOR EMGK020445 · GXY | 510(k) clearances |
| Dec 6, 1995 | PROTECTRODE SYSTEMK926094 · GXZ | 510(k) clearances |
| Nov 16, 1995 | PROTECTRODE SYSTEMS CONCENTRICK932691 · IKT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
