Gemore Technology Co, Ltd. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
FDA 510(k) cleared devices by Gemore Technology Co, Ltd. Neurology ✕
11 devices
Cleared
Aug 16, 2019
GIM-STIM OTC TENS/EMS System
Neurology
123d
Cleared
May 12, 2015
GEMORE OTC TENS
Neurology
56d
Cleared
Dec 21, 2012
GEMORE TRUE SINE INTERFERENTIAL STIMULATOR
Neurology
88d
Cleared
Dec 21, 2012
GEM-STIM COMBO STIMULATOR
Neurology
88d
Cleared
Jul 20, 2012
GEMORE TENS SYSTEM
Neurology
144d
Cleared
Jan 04, 2007
GEMORE REUSEABLE SELF ADHESIVE ELECTRODE, MODELS WIRE SERIES, SNAP SERIES AND...
Neurology
118d
Cleared
Apr 28, 2006
LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP
Neurology
88d
Cleared
Nov 17, 2004
GEM-TWIN TENS/ MODELS GM3XY/Z
Neurology
57d
Cleared
Dec 16, 2003
GM3 SERIES HV TENS, MODEL GM3X3HV (WHERE X IS PARAMETER OF DIFFERENT HOUSING)
Neurology
82d
Cleared
Dec 10, 2003
GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING)
Neurology
99d
Cleared
Dec 10, 2003
GEM-STIM TENS, MODELS GM3XY AND GM3AXY
Neurology
99d