-

Kardium Announces First Commercial Procedures with the Globe® Pulsed Field System, the World’s Most Advanced Solution for Atrial Fibrillation

This milestone marks the commercial launch of the company’s next-generation system

VANCOUVER, British Columbia--(BUSINESS WIRE)--Kardium, a private medical device company that’s advancing the way the world treats atrial fibrillation (AF), today announced the successful completion of the first commercial procedures using its integrated mapping and ablation system, the Globe Pulsed Field System, following recent approval from the U.S. Food and Drug Administration (FDA).

The inaugural U.S. procedures were performed by Dr. Devi Nair, Chief of Cardiac Electrophysiology and EP Research at St. Bernards Medical Center in Jonesboro, Arkansas. “We are very excited to offer our patients access to this groundbreaking new technology,” said Dr. Nair. “The Globe Pulsed Field System gives me greater confidence that each lesion is delivered safely and effectively, to support better outcomes for my patients while also simplifying the procedure.”

Combining high-density mapping and ablation into a single catheter enables the Globe System to deliver precise, targeted ablation using thermal contact assessment and tailored electrode selection. These capabilities allow for single-shot pulmonary vein isolation, and other customizable lesion sets, helping physicians as they strive for better outcomes for patients with atrial fibrillation.

“These first commercial procedures with the Globe System signal the beginning of a new era in AF treatment,” said Kevin Chaplin, CEO of Kardium. “We are proud to partner with leading physicians like Dr. Nair to bring the Globe Pulsed Field System into clinical practice allowing us to deliver a more personalized treatment for atrial fibrillation to improve long-term outcomes for patients.”

Data from the pivotal PULSAR study of the Globe Pulsed Field System, presented at the 2025 Heart Rhythm Society annual meeting, showed 78% freedom from atrial arrhythmia at one year in patients with paroxysmal AF patients, no device-related primary safety events and 95% lesion durability.

Following these successful first commercial procedures, Kardium will continue to expand commercial availability of the Globe Pulsed Field System across the United States, in collaboration with leading electrophysiology centers.

About Kardium

We are a rapidly growing, privately held medical solutions company with a mission to deliver the best treatment for atrial fibrillation through the Globe Pulsed Field System.

Contacts

T: +1.604.248.8891
E: Info@kardium.com

Kardium


Release Versions

Contacts

T: +1.604.248.8891
E: Info@kardium.com

More News From Kardium

Kardium receives FDA approval of the Globe® Pulsed Field System

VANCOUVER, British Columbia--(BUSINESS WIRE)--Kardium Inc., a private medical device company that’s advancing the way the world treats atrial fibrillation (AF), announced today it has received pre-market approval (PMA) for the Globe® Pulsed Field System and 510(k) clearance for both the Globe® Introducer sheath and the Globe® Pulsed Field System mapping software from the U.S. Food and Drug Administration (FDA). The Globe System is the only integrated, high-density cardiac mapping and ablation s...

Kardium Announces $250M (CA$340M) Financing to Launch Innovative Atrial Fibrillation Treatment

VANCOUVER, British Columbia--(BUSINESS WIRE)--Kardium Inc., the developer of the Globe® Pulsed Field System – an innovative treatment for atrial fibrillation (AF) – has raised US$250 million in a new financing round. The oversubscribed round was led by new investors including Janus Henderson Investors, Qatar Investment Authority (QIA), MMCAP, Piper Heartland Healthcare Capital, Eventide Asset Management, and Eckuity Capital. Existing investors also participated, including funds and accounts adv...

Kardium Announces 1-Year PULSAR IDE Study Results for Its PFA Device – the Globe® PF System

VANCOUVER, British Columbia--(BUSINESS WIRE)--Kardium Inc., a private medical device company that’s advancing the way the world treats atrial fibrillation (AF), announced late-breaking, one-year clinical trial results for its innovative pulsed field ablation (PFA) device—the Globe PF System. These pivotal findings from the PULSAR IDE study were announced at the Heart Rhythm Society (HRS) meeting in San Diego1, highlighting the safety and efficacy data of the Globe PF System, which is currently...
Back to Newsroom