Watkins-Conti Completes Stress Urinary Incontinence Yōni.Fit Device Trial

Women Owned Company xpands Leadership as it Prepares FDA Regulatory Filing to Enable Participation in $4B U.S. Adult Urinary Incontinence Market

Watkins-Conti Products, Inc. (“Watkins-Conti”), a healthcare company that develops solutions for often-overlooked issues affecting women at every stage of life, announced today that it has successfully completed a clinical trial studying the safety and effectiveness of its flagship product, Yōni.Fit. Yōni.Fit is a vaginal insert designed to manage stress urinary incontinence (SUI), the involuntary leakage of urine upon physical activity or pressure on the bladder.

Seventy one (71) participants enrolled in a randomized, controlled, single blind, multi-center study of the Yōni.Fit device in women with SUI. The study was led by urogynecologists at Stanford, NYU Langone, and Jefferson Health. Results from the study are being submitted to a peer-reviewed journal and associated medical conference held later this year. Watkins-Conti will be filing a 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) to provide reasonable assurance that the Yōni.Fit device is safe and effective for SUI. The FDA must review the submission and grant 510(k) clearance prior to commercial distribution.

“During my career, I have seen how medical innovations developed based on a person’s lived experience can make a meaningful impact in addressing the unique needs or considerations of the patients whom they intend to benefit,” said Nada Hanafi, regulatory strategy advisor at Watkins-Conti. “That is why I am delighted to support the pelvic health initiatives that Watkins-Conti Products is bringing forward to improve health outcomes.”

Watkins-Conti also announced the expansion of the Board of Directors and executive team. “Our leadership team represents the breadth of expertise and vision we need to launch our IP-protected pipeline of treatments and diagnostics for which we envision utilizing the Yōni.Fit device as a platform,” said CEO Allison L. Watkins. “Many women are conditioned to accept discomfort as an unavoidable fact of life. We seek to break that cycle by providing a range of convenient and comfortable solutions that put women in control of their health.”

The Board is composed of leaders with expertise across biosciences, health care services, and intellectual property. Allison L. Watkins (Founder & CEO) and Ross Watkins (President) are joined by the Board’s newest member, Mike Pintek (President, Nuclear & Precision Health Solutions, Cardinal Health), and Jennie Martel (Chief of Global Brand Protection, Colgate-Palmolive), Dr. Anula Jayasuriya (Private equity and venture capital executive), and John H. Marmaduke (former retail executive).

“We’re in a transformational time for women and women’s health, and I am excited to join the Watkins-Conti Products board to help them address health challenges impacting women,” said Mike Pintek. “The team is passionate about and committed to pioneering important innovative advancements in healthcare, and I look forward to guiding the company as it solidifies its vision.”

The executive team is focused on commercializing the company’s unique product pipeline. Sean Givens advises the company on financial modeling and forecasting. Nada Hanafi advises the company on regulatory strategy. She spent nearly 13 years at FDA’s Center for Devices and Radiological Health (CDRH) working on a range of products and devices and helped establish the CDRH Health of Women Program. Neil Luckianow is the Chief Commercialization Officer and advises the company on go-to-market strategies, product distribution, and customer engagement. Brooke Wigley is the Director of Operations where she oversees the day-to-day functions of the business.

SUI is a condition estimated to affect about 3 in 4 women worldwide at some point in their lives, negatively impacting quality of life and emotional well-being. SUI may get worse over time if left untreated, and may also contribute to pelvic organ prolapse.

The company has raised over $6M from angel investors and VCs. The funds have been directed towards creating quality management systems, protecting the company’s robust intellectual property portfolio, conducting clinical trials, and expanding the executive team and expert advisers.

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”