News | Wearables | December 28, 2017

Zoll and Myant Enter Strategic Research and Development Collaboration

Exclusive agreement leverages Myant fabric-based technologies for future generations of the Zoll LifeVest wearable defibrillator

Zoll and Myant Enter Strategic Research and Development Collaboration

December 28, 2017 — Zoll Medical Corp. and Myant, Inc., a high-tech advanced manufacturing company, announced they have entered an exclusive strategic multi-year agreement to jointly develop technologies that will be leveraged in future generations of the Zoll LifeVest wearable defibrillator. The LifeVest is worn by patients at risk of sudden cardiac death (SCD), providing protection during their changing condition and while permanent SCD risk has not been established.

The LifeVest was approved by the U.S. Food and Drug Administration (FDA) in 2001. Recommended use of the wearable defibrillator is included in the 2017 American Heart Association (AHA)/American College of Cardiology (ACC)/Heart Rhythm Society (HRS) Guideline for Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death.

The LifeVest is used for a wide range of patient conditions or situations, including following a myocardial infarction, before or after coronary revascularization, and for those with cardiomyopathy or congestive heart failure that places them at particular risk. The technology allows patients to return to their common activities of daily living, while having the peace of mind that they are protected from SCD. The LifeVest continuously monitors the patient’s heart and, if a life-threatening heart rhythm is detected, the device delivers a treatment shock to restore normal heart rhythm.

Myant focuses on advancing human connectedness to the Internet of Things by designing, developing and producing connected textile-based products.

Read the article "Zoll LifeVest Shows 97 Percent One-Year Survival for High-Risk Patients"

For more information: www.zoll.com


Related Content

News | Defibrillator Monitors

July 28, 2023 — GE HealthCare is recalling malfunctioning TruSignal sensors that may reduce the amount of energy sent to ...

Home July 28, 2023
Home
News | Defibrillator Monitors

August 3, 2022 — A defibrillator administers a therapeutic shock to a patient's heart in life-threatening circumstances ...

Home August 03, 2022
Home
News | Defibrillator Monitors

August 1, 2022 — A study from the University of Warwick has found that school-based defibrillators (AEDs) that are ...

Home August 01, 2022
Home
News | Defibrillator Monitors

June 23, 2020 — Philips announced the U.S. Food and Drug Administration (FDA) has granted premarket approval (PMA) for ...

Home June 23, 2020
Home
News | Defibrillator Monitors

April 24, 2020 — The U.S. Food and Drug Administration (FDA) has lifted its injunction prohibiting the manufacturing and ...

Home April 24, 2020
Home
News | Defibrillator Monitors

January 13, 2020 — Stryker announced it is launching a voluntary field action on specific units of the LifePAK 15 ...

Home January 13, 2020
Home
Technology | Defibrillator Monitors

June 19, 2019 — Philips announced the U.S. Food and Drug Administration (FDA) has approved the company’s premarket ...

Home June 19, 2019
Home
News | Defibrillator Monitors

April 5, 2019 — Medical device startup HeartHero was the winner in the Innovation Challenge at the 2019 American College ...

Home April 05, 2019
Home
Feature | Defibrillator Monitors

February 4, 2019 — Stryker announced Feb. 1, the company is launching a voluntary field action on specific units of the ...

Home February 04, 2019
Home
Feature | Defibrillator Monitors | Michael J. Mirro, M.D.

Following the Vest Prevention of Early Sudden Death Trial (VEST) presentation at the 2018 American College of Cardiology ...

Home July 10, 2018
Home
Subscribe Now