Medtronic plc announced that it has obtained approval from the U.S. Food and Drug Administration (FDA) for Aurora EV-ICD MRI SureScan (Extravascular Implantable Cardioverter-Defibrillator) and Epsila EV MRI SureScan to offer the advantages of conventional, transvenous ICDs in terms of saving lives by providing anti-tachycardia pacing (ATP), backup (pause-prevention) pacing therapy, and life-saving defibrillation.
Abbott received approval from the U.S. Food and Drug Administration (FDA) for Gallant implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) devices with Bluetooth technology and a new patient smartphone app for better remote monitoring for patients with cardiac rhythm abnormalities.
Author Credits: Radhika Gupta, Shivam Bhutani
Report ID: 874
Published Date: Nov 17, 2023
Report Format: PDF, PPT
Frequently Asked Questions (FAQ)
Rising incidence of heart attacks across the globe and the growing technological advancement in cardiology are the major factors driving the growth of the market.
The market size of Wearable Cardioverter Defibrillators is anticipated to attain a CAGR of 6% over the forecast period, i.e., 2024 – 2036.
The major players in the market are ZOLL Medical Corporation, Element Science Inc., Medtronic plc, Kestra Medical Technologies, Inc., Abbott, Boston Scientific Corporation, LivaNova plc, Koninklijke Philips N.V., Nihon Kohden Corporation and General Electric Company., and others.
The peripartum cardiomyopathy segment is anticipated to garner the largest market size by the end of 2036 and display significant growth opportunities.
The market in the North American region is projected to hold the largest market share by the end of 2036 and provide more business opportunities in the future.