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LivaNova PLC

LivaNova PLC, a medical technology company, designs, develops, manufactures, markets, and sells products, therapies, and services. The company operates in two segments, Cardiopulmonary and Neuromodulation. The Cardiopulmonary segment provides cardiopulmonary products, including heart-lung machines, oxygenators, autotransfusion systems, perfusion tubing systems, cannula, and other related accessories, as well as services related products. The Neuromodulation segment offers VNS Therapy System, an implantable pulse generator and connective lead that stimulates the vagus nerve, surgical equipment to assist with the implant procedure, and equipment and instruction manuals; and devices that deliver neuromodulation therapy for treating drug-resistant epilepsy and depression. This segment also includes the development and clinical testing of aura6000 system for treating obstructive sleep apnea. It serves perfusionists, neurologists, neurosurgeons, hospitals, other healthcare professionals and medical institutions, and healthcare providers. The company sells its medical devices through direct sales representatives, agents, and independent distributors in the United States, the United Kingdom, Germany, France, Italy, the Netherlands, Spain, Belgium, Poland, Sweden, Switzerland, Austria, Norway, Portugal, Finland, Denmark, and internationally. LivaNova PLC was incorporated in 2015 and is headquartered in Gloucester, the United Kingdom.

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LivaNova raises 2026 guidance after record second quarter

LivaNova reported record second-quarter revenue and earnings per share and raised its full-year 2026 outlook. Revenue rose 9.8% on a constant currency basis to $391 million, with Cardiopulmonary revenue up 10% to $222 million and Epilepsy revenue up 10%. The company now expects full-year revenue growth of 8% to 9%, up from 7% to 8%, and adjusted diluted earnings per share of $4.30 to $4.40, up from prior guidance. LivaNova also announced a long-term supply agreement with Thermo Fisher Scientific for a critical oxygenator component and said it expects to submit a PMA supplement for its next-generation OSA system between the second half of 2026 and the first half of 2027.
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LivaNova PolySync Programming Boosts OSA Response Rate to 84.5%

LivaNova announced new data from its PolySync substudy showing that its PolySync programming algorithm increased the cumulative apnea-hypopnea index response rate from 65% to 84.5% in patients with moderate-to-severe obstructive sleep apnea treated with proximal hypoglossal nerve stimulation therapy delivered by the aura6000 System. The findings were presented at SLEEP 2026. The PolySync substudy evaluated patients who did not meet responder criteria after one year of individual-contact stimulation in the OSPREY randomized controlled trial, which previously demonstrated a 65% responder rate. The aura6000 System received FDA premarket approval in March. LivaNova is developing a next-generation OSA device with MRI compatibility, remote configuration, and a rechargeable battery with up to 15 years of life, and plans to file a PMA supplement submission in the second half of 2026.
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