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Efemoral Medical’s lead product, the Efemoral Vascular Scaffold System (EVSS), has demonstrated promising early results in first-in-human studies. The EVSS achieved 0% post-procedure residual stenosis—the lowest ever reported for a femoropopliteal trial—and maintained a mean minimal lumen diameter of 4.74 mm at six months, the highest reported to date. The system aims to provide durable outcomes without permanent implants and has received FDA Breakthrough Device designation for treating chronic limb-threatening ischemia.
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