Abbott LaboratoriesAbbott's Amulet 360 received CE Mark, a regulatory approval for its next-generation device, with positive clinical data and planned rollout.

Abbott announced it has received CE Mark for its next-generation Amulet 360 Left Atrial Appendage Occluder, designed to reduce stroke risk in patients with non-valvular atrial fibrillation. The device, which seals the left atrial appendage to prevent blood clots, builds on Abbott's first-generation LAA occluder with a softer, more conformable lobe and smaller anchors to treat a wider range of anatomies. Clinical data from the VERITAS Study, involving 400 patients at over 30 hospitals, showed successful implantation in 99.8% of patients, no early complications, and complete closure in 93.9% of patients at 45 days. The first European procedures were completed in Germany and Denmark, with broader rollout planned in coming weeks. This approval marks Abbott's fourth major electrophysiology approval in just over a year, following the Volt PFA System and TactiFlex Duo.
Abbott LaboratoriesAbbott's Amulet 360 received CE Mark, a regulatory approval for its next-generation device, with positive clinical data and planned rollout.