# K062675: Gemore Reuseable Self Adhesive Electrode, Models Wire Series, Snap Series and Double Side Series

- Pathway: 510(k) (Traditional)
- Applicant: Gemore Technology Co, Ltd.
- Decided: Jan 4, 2007 after 118 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K945676 (1995). 8 ancestors in all.
21 later devices descend from it; 2 cite it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052875: Prostim Reusable Neurostimulation Electrodes, Summit Manufacturing, LLC (2005) Summary page 1.
- K050788: Everlife, Everlife Medical Instrument Co., Ltd. (2005) Summary page 1.

## Most influential descendants
- K083302: Lifecare Electrodes (2009), 14 descendants of its own
- K130987: Valutrode Neurostimlation Electrodes (2013), 10 descendants of its own
- K150971: Zekang Self-adhesive Electrode (2015), 5 descendants of its own
- K082065: Well Life Self Adhesive Electrode / Models: CM, FA, PU and SP (2009), 5 descendants of its own
- K152648: Ennova Self-adhesive Electrode (2016), 4 descendants of its own

## Indications for use
The Gemore Reuseable Self Adhesive Electrode / Wire series, Snap series, and Double side series are intended for use as a disposable, conductive adhesive interface between the patient's skin and the Electrical Stimulator. Gemore Reuseable Self Adhesive Electrode /Wire series, snap series, and double side series are designed and intended to be used with marketed Electrical Stimulators, i.e. TENS (Transcutaneous Electrical Nerve Stimulation), MENS (Microcurrent Electrical Nerve Stimulation), EMS (Electrical Muscular Stimulation), IF (Interferential) and PGS (Pulsed Galvanic Stimulation).

Source page: https://510kreport.com/device/K062675
Methodology: https://510kreport.com/methodology