News | Ablation Systems | April 16, 2019

CardioFocus Announces European CE Mark Approval Of HeartLight X3 System

Third-generation technology employs RAPID mode for more precise control during pulmonary vein isolation

CardioFocus Announces European CE Mark Approval Of HeartLight X3 System

April 16, 2019 — CardioFocus Inc. announced the European CE Mark approval of the HeartLight X3 Endoscopic Ablation System.

The HeartLight X3 System is a third-generation technology building upon the advanced features of the HeartLight Endoscopic Ablation System, which performs pulmonary vein isolation (PVI) using laser energy to create lines of scar tissue to block the abnormal electrical pathways that cause atrial fibrillation (AFib). Using direct tissue visualization, titratable laser energy and compliant balloon technology, the HeartLight X3 System's RAPID mode leverages a precise motor control system that enables uninterrupted, high-speed, circumferential lesion creation under direct control of the physician, resulting in consistently reduced procedure times.

More than 33 million patients worldwide suffer from AFib, the most common type of cardiac rhythm disorder.1, 2 In Europe alone, it is estimated that the number of patients will rise to 14-17 million by 20303.

"Our clinical results using the HeartLight X3 System have been outstanding, with unprecedented treatment speed and precise lesion creation," said Boris Schmidt, M.D., an investigator in the pivotal confirmatory trial at Cardioangiologisches Centrum Bethanien in Frankfurt, Germany. "Based on our experience with the device, we feel confident that the HeartLight X3 System is poised to change the way AFib ablation is performed in Europe."

In the pivotal confirmatory evaluation of 60 patients, the HeartLight X3 System consistently achieved very rapid PVI, in as few as 3 minutes for a single vein. The trial also found that the system has the potential to complete all required ablations in less than 20 minutes.

Commercial introduction of the HeartLight X3 System in Europe will begin immediately. Current users of the HeartLight platform may start using HeartLight X3 technology after a simple upgrade.

The HeartLight X3 System is only approved for use in Europe. The HeartLight X3 System is not available for sale in the U.S.

For more information: www.cardiofocus.com

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