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Since two PFA products received FDA approval at the end of last year and the beginning of this year, the use of PFA products to treat atrial fibrillation has become highly popular in U.S. hospitals, with doctors eager to use PFA for patient treatment.
In addition to the positive outlook from hospital doctors on PFA, the U.S. market also highly values PFA, which is expected to replace radiofrequency ablation and cryoablation in the near future. According to predictions by Industry and Wall Street, with its unique technical advantages, PFA will soon become the mainstream ablation technology for treating atrial fibrillation.
A survey of 25 electrophysiologists in the United States shows: In the next 12 months,The use of PFA will increase from 9% today to over 30%.Most doctors said that PFA would enable them to perform more heart surgeries.


Johnson & Johnson Market ShareFrontal Loss NotThe largest is Abbott. Due to Abbott's relatively late deployment in PFA technology, it is unable to quickly respond to the fierce competition from innovative PFA products like FARAPULSE and PulseSelect. Therefore, the market expects its market share to drop significantly. Moreover, the decline will be much greater than that of Johnson & Johnson.Johnson & Johnson's PFA product VARIPULSE has received CE and Japanese approval, with FDA approval expected in the second half of this year.VARIPULSE Launch.
Abbott's first PFA productVolt PFA has just received FDA approval for the IDE study. If the clinical study goes smoothly,Volt PFA will not be available on the market until 2027. By then, the entire electrophysiology market will have undergone tremendous changes, and Abbott could potentially shift from being a mainstream player to being categorized as "others." Despite this...Abbott believesVolt PFA has technical advantages that other PFA products do not possess, enabling it toAddress the limitations of existing PFA products.


For Medtronic, the electrophysiology ablation market in the next 12 months is a mix of opportunities and challenges. The positive aspect is thatPulseSElect is the first FDA-approved product and will also leveragePulseSElect and other technologies capture the radiofrequency ablation market. Concerns arise regarding its cryoablation.The Arctic Front series will be significantly impacted by PFA. According to statistical analysis.In the next 12 months, the market share of radiofrequency catheter ablation will drop from nearly 68% to less than 54% (a decline of over 20%).The share of cryoablation catheters is expected to drop from around 23% to below 16% (a decrease of over 30%). Medtronic'sPulseSThe increase in PFA sales will be offset by losses in the cryoablation market.Therefore, the market expects its performance in the electrophysiology ablation market over the next 12 months.Increase in market shareLess than 1%.

