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ProACT™ Adjustable Continence Therapy for Men has been commercially available since FDA approval in November 2015 with over 8,500 implants worldwide as of late-stage reporting. Clinical trials are ongoing for ACT® Adjustable Continence Therapy for Women under an FDA Investigational Device Exemption to evaluate safety and efficacy. The company’s devices are minimally invasive, adjustable after implantation without further surgery, and have demonstrated excellent results internationally. Over 16,000 patients have received Uromedica implants globally.
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