Johnson & Johnson launches dual-energy cardiac platform in Europe
Johnson & Johnson launched the Dual Energy THERMOCOOL SMARTTOUCH SF Platform in Europe, integrating pulsed field and radiofrequency energy for cardiac ablation. The system aims to enhance procedural versatility and personalized treatment. Clinical data from the SmartfIRE study indicates an 86.9% effectiveness rate at 12 months.

*this image is generated using AI for illustrative purposes only.
Johnson & Johnson today announced the commercial launch of the Dual Energy THERMOCOOL SMARTTOUCH SF (DE STSF) Platform in Europe, expanding physician access to a dual-energy catheter ablation solution. The platform is designed to provide personalized care across workflows, anatomies, and procedural strategies by combining pulsed field and radiofrequency energy delivery in a unified system.
The DE STSF Platform integrates the Dual Energy THERMOCOOL SMARTTOUCH SF Catheter, an irrigated contact-force sensing catheter, with the TRUPULSE Generator. This configuration enables electrophysiologists to deliver both radiofrequency (RF) and pulsed field (PF) energy through a single catheter during the same procedure. The system leverages CARTO integration, ultra high-density mapping solutions, and intracardiac ultrasound imaging to provide advanced electro-anatomical mapping, catheter visualization, contact-force feedback, and PF/RF Index guidance.
Built upon the THERMOCOOL SMARTTOUCH SF platform, which has treated more than a million patients worldwide, the new system maintains a familiar point-by-point workflow. It allows physicians to switch between RF and PFA seamlessly, offering greater versatility to adjust treatment to different patient anatomies and clinical needs. This flexibility is intended to support procedural control and reproducible lesion creation.
"DE STSF is a welcome addition to the EP lab because it allows physicians to incorporate new technology based on the gold RF standard smarttouch SF platform while maintaining familiar workflows with greater versatility by seamlessly switching between RF and PFA," said Nicolas Derval, M.D., of Bordeaux, France. "This flexibility also provides greater ability to adjust treatment to different patient anatomies, clinical needs and procedural goals while increasing safety in ablating the posterior wall for example."
Clinical data supporting the platform include 12-month findings from the SmartfIRE first-in-human study. The study demonstrated 86.9% effectiveness among patients treated with high adherence to the recommended workflow and PF/RF Index guidance. Additionally, the study showed clinically meaningful improvements in quality of life and reductions in cardiovascular-related hospitalizations and antiarrhythmic drug use.
"No two atrial fibrillation patients are the same, which is why personalized treatment and procedural versatility matter," said Ricardo Martin, President EMEA, Electrophysiology, MedTech, Johnson & Johnson. "The launch of the Dual Energy THERMOCOOL SMARTTOUCH SF Platform reflects our continued commitment to providing physicians with a broad range of treatment options."
Key Clinical Data
| Study | Duration | Effectiveness | Key Outcomes |
|---|---|---|---|
| SmartfIRE | 12 months | 86.9% | Improved quality of life, reduced hospitalizations, reduced antiarrhythmic drug use |
What is the anticipated timeline for regulatory approval and commercial launch of the DE STSF Platform in key markets such as the United States?
How will the pricing strategy for this dual-energy system compare to existing single-energy ablation solutions, and will reimbursement policies support its adoption?
What are the long-term competitive implications for Johnson & Johnson's electrophysiology portfolio if other device manufacturers successfully integrate pulsed field and radiofrequency technologies?






























