geko

Device Name

Neuromuscular Stimulation Device Pack

Model / Reference

W-3 pack, W3RW01-07

Primary DI / UDI-DI

05060294772095, 05060294771524

Basic UDI-DI

506029477W3pkEZ

EMDN Code

N0199 Encephalic and peripheral nervous system devices - other

Device Class

Class IIa

Medical Purpose

• to increase blood circulation • for the treatment of oedema • for promoting wound healing • for the treatment of venous insufficiency and ischemia

EUDAMED SRN

UK-PR-000040065

• geko W-2

  Class II

  FDA 510(k) K212762 Active Cleared 29 Nov 2021

• geko™ W-2

  Class II

  FDA 510(k) K193045 Active Cleared 18 Jan 2020

• geko T-3 Neuromuscular Stimulator

  Class II

  FDA 510(k) K181059 Active Cleared 23 May 2018

• geko T-2 and geko T-3 Neuromuscular Stimulators

  Class II

  FDA 510(k) K191113 Active Cleared 18 Sep 2019

• geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators

  Class II

  FDA 510(k) K163125 Active Cleared 10 Apr 2017

• geko T-2 Neuromuscular Stimulator

  Class II

  FDA 510(k) K152677 Active Cleared 23 Oct 2015

See all devices from Firstkind Limited →