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Providence, RI, Oct. 01, 2021 (GLOBE NEWSWIRE) — Signati Medical, Inc. is pleased to announce that LeRoy Jones, MD and Ryan Owen, MD have joined their Clinical Advisory Board. Their combined experience and expertise in men’s health as renowned board certified urologists make them an invaluable addition to the vision of Signati Medical, Inc.

About LeRoy Jones, MD
Dr. LeRoy Jones is currently in private practice with Urology San Antonio in San Antonio Texas. He opened the Center for Male Health and Wellness, a division of Urology San Antonio. He is also a Clinical Associate Professor at the University of Texas Health Science Center in San Antonio. Previous academic appointments include The University of New Mexico Health Science Center and at the Baylor College of Medicine in Houston, Texas. Dr. Jones received his medical education at Washington University St. Louis. Surgical and Urological training was at the Johns Hopkins Hospital and the Baylor College of Medicine in Houston respectively.

Dr. Jones is considered an authority in the field of sexual medicine, having performed over 3000 prosthetic surgeries. He has numerous publications in the field of sexual medicine. Dr. Jones is internationally recognized and has taught surgery in many countries all over the world. He is the past president of The Society of Urologic Prosthetic Surgeons and is an active member of the Sexual Medicine Society of North America.

About Ryan Owen, MD
Dr. Ryan Owen is fellowship trained in male reproductive health and microsurgery. His medical journey began at Texas Tech University School of Medicine. After graduation, he began a Urology residency at The University of Tennessee and then completed an additional year of fellowship at the University of North Carolina. Currently living in Lubbock, Texas, his practice focuses on a wide range of urologic disease with a focus on male reproduction. He is an assistant professor at the Texas Tech University Urology residency program, where he has introduced residents and students to clinical and surgical aspects of male reproductive health.

Dr. Owen has contributed numerous publications toward the field of urology spanning from testosterone supplementation and erectile dysfunction to genetic testing for men seeking fertility. Given his focus toward the advancement of men’s health, Dr. Owen has joined the Signati Medical team with the ambition to help create a safe and efficient method to perform a non-invasive vasectomy procedure.

To read more about the Clinical Leadership Advisors, please visit www.signatimed.com.

About Signati Medical
Signati Medical is a medical device company that endeavors to take vasectomy to a new level of comfort, safety, and speed. A medical device company dedicated to advancing men’s health, Signati plans to launch the first innovation in vasectomy in more than 20 years with a procedure that would be fast for physicians and comfortable for patients. The Signati procedure, designed to take just minutes, could be done right in the urologist’s office and would offer advantages for patients including easier recovery compared to some current vasectomy techniques.
To learn more, visit www.signatimed.com.

Not approved by the Food and Drug Administration (FDA). These statements and the subject product have not been evaluated by the Food and Drug Administration (FDA). This product is not intended to diagnose, treat, cure, or prevent any disease. The device is not currently being marketed, nor is it available for sale in any country.

Signati Medical Announces Phase 2 Study Showing a New Bipolar Radio-Frequency Sealing Tool for Trans-scrotal Vasectomy.

Initial animal study revealed effective vas deferens sealing.

May 24,2021—Signati Medical, Inc., a medical device company focused on advancing men’s health with a proprietary bipolar radio frequency sealing platform, announced today that the company initiated a second preclinical study on New Zealand rabbits. Signati has developed a unique impedance detection algorithm and was conducting this second preclinical evaluation to further correlate the radio-frequency energy delivered to the surgical site with effective vas deferens sealing. The ability of the system to monitor impedance eliminates procedure guesswork, creating effective closure of the vas deferens through scrotal skin (trans-scrotal) and improving the surgical outcome by minimizing damage to the surrounding tissue.

This additional preclinical study will seek to expand the positive findings of Signati’s initial preclinical study on New Zealand rabbits. In the initial study, validated laboratory and histological assessments were conducted in a rabbit model to demonstrate that the Signati Medical system had been designed with optimal electrosurgical radio frequency (RF) energy parameters and electrode geometry for creating an effective seal in the vas deferens. Post procedure healing was also monitored to confirm that thermal spread to surrounding tissue did not cause damage. The methods and conditions of the first study remained the same in the second study, with the addition of rabbit models conducted using a no scalpel method. This was added to confirm that sealing parameters are effective should this method be preferred based on clinical preference and/or need. Post treatment histological slides have confirmed positive vas deferens sealing.

Signati’s Chief Medical Officer, Dr. Gerard Henry, was encouraged by the success of the preclinical study results stating, “We look forward to conducting further studies seeking to validate and build on the initial success of Signati’s preclinical results, which demonstrated that our custom engineered RF bipolar generator creates effective vas deferens sealing. We believe our proprietary handpiece, electrode design, and impedance detection algorithm has the potential to become a leading treatment option when performing vessel sealing, such as the vas deferens. We look forward to submitting this data in a 510k to the FDA, and the results we have seen thus far make us very confident in Signati Medical’s novel approach to trans-scrotal vessel sealing vasectomy.”

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Not approved by the Food and Drug Administration (FDA).
These statements and the subject product have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. The device is not currently being marketed, nor is it available for sale in any country.

Signati Medical Announces Clinical Advisors

Signati Medical Inc. is pleased to announce the following doctors have joined their Clinical Advisory Board: Gerard Henry, MD; Tariq S. Hakky, MD; Joel L. Marmar, MD; Rahul Mehan, MD; Michel Labrecque, MD, PhD.

About The Clinical Advisors
Gerard Henry, MD is Signati’s Chief Medical Officer, the #1 US AMS IPP implanter for the last ten years, and is the #1 published author on IPPs in the world over the last ten years.

Tariq S. Hakky, MD is a world-renowned microsurgeon and a diplomate of the American Board of Urology. He is Baylor College of Medicine fellowship-trained in male infertility and andrology, and the owner and founder of Atlanta Cosmetic Urology.

Michel Labrecque, MD, PhD is an emeritus professor from the Department of Family and Emergency Medicine at Laval University, Quebec City, Canada. As of 2020, he has performed more than 35,000 vasectomies, and was the first physician to practice the No Scalpel Vasectomy (NSV) in Canada in 1992.

Rahul Mehan, MD is the founder of East Valley Urology (EVU) Center in Mesa, Arizona and a board-certified urologist focusing on Urologic oncology. He is a skilled surgeon with extensive training in testicular, renal, prostate, and bladder cancers at EVU Center.

Joel L. Marmar, MD is a highly respected urologist with a career spanning nearly 40 years. He is an author of AUA Vasectomy Guidelines published in 2012, and the developer of the “In-Line Vasectomy” (ILV) technique—an improved method for performing a no-scalpel vasectomy.

To read more about the Clinical Leadership Advisors, please visit www.signatimed.com.

About Signati Medical
Signati Medical is a medical device company that endeavors to take vasectomy to a new level of comfort, safety, and speed. A medical device company dedicated to advancing men’s health, Signati plans to launch the first innovation in vasectomy in more than 20 years with a procedure that would be fast for physicians and comfortable for patients. The Signati procedure, designed to take just minutes, could be done right in the urologist’s office and would offer advantages for patients including easier recovery compared to some current vasectomy techniques.
To learn more, visit www.signatimed.com.

Not approved by the Food and Drug Administration (FDA). These statements and the subject product have not been evaluated by the Food and Drug Administration (FDA). This product is not intended to diagnose, treat, cure, or prevent any disease. The device is not currently being marketed, nor is it available for sale in any country.