Gemore Technology Co, Ltd.
Gemore Technology Co, Ltd. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2019.
Top product codes for Gemore Technology Co, Ltd.
Recent clearances by Gemore Technology Co, Ltd.
- K190988 — GIM-STIM OTC TENS/EMS System
- K150681 — GEMORE OTC TENS
- K122944 — GEMORE TRUE SINE INTERFERENTIAL STIMULATOR
- K122948 — GEM-STIM COMBO STIMULATOR
- K120569 — GEMORE TENS SYSTEM
- K102933 — GEM-TONE BODY TRAINING SYSTEM
- K102926 — GEMORE MUSCLE CONDITIONER
- K091833 — GEM-STONE ABDOMINAL TRAINING SYSTEM; MODEL GEM-TONE 310PE/320PE/330PE/340PE/350PE.
- K062675 — GEMORE REUSEABLE SELF ADHESIVE ELECTRODE, MODELS WIRE SERIES, SNAP SERIES AND DOUBLE SIDE SERIES
- K060222 — LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP
- K042559 — GEM-TWIN TENS/ MODELS GM3XY/Z
- K032994 — GM3 SERIES HV TENS, MODEL GM3X3HV (WHERE X IS PARAMETER OF DIFFERENT HOUSING)
- K032719 — GM3 SERIES IF TENS, MODEL GM3X2IF (WHERE X IS A PARAMETER OF DIFFERENT HOUSING)
- K032720 — GEM-STIM TENS, MODELS GM3XY AND GM3AXY
Data sourced from openFDA. This site is unofficial and independent of the FDA.