Abbott Amulet 360 shows strong one-year LAA closure in VERITAS study
Nov 2, 2026, 9:15 AM EST1 sourcesAI-analyzed
Why it may matterVerify against the original reporting
Strong one-year efficacy signals (96.3% closure) and stroke-free rates support ABT's strategic AFib device narrative, though US regulatory status limits immediate revenue upside; history shows clinical data can lift sentiment and multiples even before approvals, yet actual cash flow hinges on US clearance and reimbursement.
AI summary
What happened, with direct paths to the underlying reporting
Abbott reported one-year VERITAS results for Amulet 360 showing durable LAA closure (96.3% zero-leak) and low stroke risk, with over 98% stroke/systemic embolism-free and CV mortality-free at 12 months. CE Mark approval arrived in August 2026; US approval remains investigational, underscoring a regulatory hurdle before near-term revenue realization.
Ischemic stroke/systemic embolism-free >98% at one year; mortality-free >98%.
CE Mark approved August 2026; US use is investigational.
Amulet 360 design: softer lobe and outer disc improve sealing across anatomies.
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