Abbott LaboratoriesFDA approval of new dual-energy ablation catheter expands product portfolio.

Abbott has received U.S. Food and Drug Administration approval for its TactiFlex Duo Ablation Catheter, Sensor Enabled, a dual-energy device that combines pulsed field ablation and radiofrequency energy in a single catheter to treat complex cases of atrial fibrillation. The approval, announced September 8, 2026, is based on results from the FlexPulse IDE study, which showed favorable safety and effectiveness in patients with paroxysmal AFib. Abbott will begin commercial cases across the country in the coming weeks. This marks the company's fifth major electrophysiology approval in just over a year, following European approvals of the Amulet 360 and TactiFlex Duo, and U.S. and European approvals of the Volt PFA System in 2025. The catheter integrates with Abbott's EnSite X EP System, which provides real-time feedback and a PFA Index to guide lesion formation.
Abbott LaboratoriesFDA approval of new dual-energy ablation catheter expands product portfolio.