New Delhi (India), July 27: In a major stride towards improving women’s healthcare, Nesa Medtech, a prominent startup in women’s health, has announced that its groundbreaking Fibroid Mapping Reviewer Application (FMRA) has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). The FMRA technology represents a significant advancement that will aid physicians in planning minimally invasive image-guided treatments for uterine fibroids.
The FMRA’s clearance is expected to have a profound impact on the treatment offered for uterine fibroids, leading to the development of subsequent devices offering minimally invasive treatment options to patients with symptomatic uterine fibroids. By providing accurate and detailed information on fibroid location and dimensions, physicians can tailor treatment plans to suit each patient’s unique condition, improving overall outcomes and patient satisfaction.
Welcoming the FDA 501(K) clearance for Nesa’s solution, C-CAMP Director and CEO Dr Taslimarif Saiyed said, “Women’s health is a top priority for any universal healthcare program across the globe. We are delighted that with this nod from FDA, Nesa’s FMRA technology, as an indigenous Make in India story is a resounding success for India’s indigenous medical technology sector.”
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