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Pulsed-field ablation (PFA) with a system encompassing the Varipulse catheter and Trupulse generator with integrated 3D electroanatomic mapping (all Biosense Webster) safely and effectively treats ...

“Out of an abundance of caution,” Johnson & Johnson MedTech has temporarily paused the use of its Varipulse field ablation system in the United States, the company announced. The move comes after the ...

After more than a monthlong pause in response to four neurovascular events linked to its Varipulse pulsed-field ablation system, Johnson & Johnson announced late last week that it will resume use of ...

Johnson & Johnson MedTech will enter the U.S. pulsed field ablation market following an FDA green light for its Varipulse platform for the treatment of atrial fibrillation. The sector has seen massive ...

Johnson & Johnson (J&J) has reported interim 12-month results from the VARIPURE study, assessing the effectiveness and safety of its Varipulse pulsed field ablation (PFA) platform in first-time users.

On Wednesday, Johnson & Johnson (NYSE:JNJ) said it has temporarily paused all U.S. cases using its Varipulse pulsed field ablation (PFA) system. Pulsed-field ablation (PFA) is a non-thermal procedure ...

Bengaluru: Johnson & Johnson said on Wednesday it had temporarily paused the rollout of its Varipulse heart device in the United States, as the company investigates four reported stroke events. The ...

Johnson & Johnson said the U.S. rollout of the Varipulse pulsed field ablation platform is back on after an investigation found the devices operate as intended. Can artificial intelligence (AI) ...

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