Abbott introduces its FDA-approved TactiFlex Duo ablation catheter
The sensor-enabled device delivers precision and flexible treatment options for patients seeking minimally invasive solutions for atrial fibrillation.
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Global healthcare products and technologies company
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In short: Abbott received key device approvals for heart and diabetes care and settled long-running infant formula litigation for $670 million.
The sensor-enabled device delivers precision and flexible treatment options for patients seeking minimally invasive solutions for atrial fibrillation.
The TactiFlex Duo combines pulsed field and radiofrequency ablation. Trial data show 92.6% patients remained arrhythmia-free at follow-up, with a 98.3% safety profile and no major adverse events.
Designed to seal the heart's left atrial appendage, the device reduces stroke risk without long-term blood thinners, backed by high closure rates from the VERITAS clinical trial.
The test provides another screening option for up to 60 million unscreened eligible Americans, complementing existing Cologuard tests.
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Abbott's TactiFlex Duo provides pulsed-field ablation and radiofrequency to offer greater flexibility in treating atrial fibrillation.
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