Company ยท TW
Gemore Technology Co, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2019. Name variants (Inc, Corp, punctuation) are merged.
14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 16, 2019 | K190988 | GIM-STIM OTC TENS/EMS System Gemore Technology Co, Ltd., TW | NUH |
| May 12, 2015 | K150681 | GEMORE OTC TENS Gemore Technology Co, Ltd., TW | NUH |
| Dec 21, 2012 | K122948 | GEM-STIM COMBO STIMULATOR Gemore Technology Co, Ltd., TW | GZJ |
| Dec 21, 2012 | K122944 | GEMORE TRUE SINE INTERFERENTIAL STIMULATOR Gemore Technology Co, Ltd., TW | LIH |
| Jul 20, 2012 | K120569 | GEMORE TENS SYSTEM Gemore Technology Co, Ltd., TW | GZJ |
| Sep 2, 2011 | K102933 | GEM-TONE BODY TRAINING SYSTEM Gemore Technology Co, Ltd., TW | NGX |
| Aug 25, 2011 | K102926 | GEMORE MUSCLE CONDITIONER; Gemore Technology Co, Ltd., TW | NGX |
| Oct 16, 2009 | K091833 | GEM-STONE ABDOMINAL TRAINING SYSTEM; MODEL GEM-TONE 310PE/320PE/330PE/340PE/350PE. Gemore Technology Co, Ltd., TW | NGX |
| Jan 4, 2007 | K062675 | GEMORE REUSEABLE SELF ADHESIVE ELECTRODE, MODELS WIRE SERIES, SNAP SERIES AND DOUBLE SIDE SERIES Gemore Technology Co, Ltd., TW | GXY |
| Apr 28, 2006 | K060222 | LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP Gemore Technology Co, Ltd., TW | NUH |
| Nov 17, 2004 | K042559 | GEM-TWIN TENS/ MODELS GM3XY/Z Gemore Technology Co, Ltd., TW | GZJ |
| Dec 16, 2003 | K032994 | GM3 SERIES HV TENS, MODEL GM3X3HV (WHERE X IS PARAMETER OF DIFFERENT HOUSING) Gemore Technology Co, Ltd., TW | GZJ |
| Dec 10, 2003 | K032720 | GEM-STIM TENS, MODELS GM3XY AND GM3AXY Gemore Technology Co, Ltd., TW | GZJ |
| Dec 10, 2003 | K032719 | GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING) Gemore Technology Co, Ltd., TW | LIH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||