Cardiofocus, Inc.
4 devices · 160 adverse event reports · 2 deaths reported · 1 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- HeartLight 18-5000Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 recall55 reports
- HeartLight 18-2531-N250Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 death69 reports
- HeartLight 18-3356CATHETER, STEERABLE20 reports
- HeartLight 18-4000-27ACatheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation1 death16 reports