Gemore Technology Co, Ltd.
FDA 510(k) medical device clearances.
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.