Gemore Technology Co, Ltd. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Gemore Technology Co, Ltd. has 14 FDA 510(k) cleared neurology devices. Based in Tan Shui, Taipei Hsien, TW.
Historical record: 14 cleared submissions from 2003 to 2019.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Gemore Technology Co, Ltd.
14 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
Sep 02, 2011
GEM-TONE BODY TRAINING SYSTEM
Physical Medicine
333d
Cleared
Aug 25, 2011
GEMORE MUSCLE CONDITIONER
Physical Medicine
325d
Cleared
Oct 16, 2009
GEM-STONE ABDOMINAL TRAINING SYSTEM
Physical Medicine
116d
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