(HealthDay) -- "Surgeon-tailored" polypropylene mesh (STPM) repair using a transobturator midurethral sling procedure alone or in combination with pelvic organ prolapse repair is an effective ...
In a Health Notification issued in October 2008 and updated in July 2011, the U.S. Food and Drug Administration (FDA) warned of serious complications associated with transvaginal placement of surgical ...
The Food and Drug Administration has issued a new warning about a medical device many say never should have been implanted in millions of women. In January, the FDA re-classified transvaginal mesh, a ...
The U.S.Food and Drug Administration has moved to strengthen regulations on vaginal mesh, a controversial medical device used to treat pelvic organ prolapse, a condition that can occur after ...
There are many questions about the optimal way to evaluate and manage the outlet in clinically continent women with high-grade pelvic organ prolapse (POP). Women with POP are thought to be at high ...
CHICAGO — The ban on further sales of transvaginal mesh for pelvic organ prolapse (POP) imposed by the US Food and Drug Administration (FDA) last month has some people cheering, some saying that an ...
New York, June 22, 2021 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Urinary Incontinence & Pelvic Organ Prolapse Devices And Equipment Global Market Report 2021: COVID-19 ...
American Medical Systems Holdings, Inc. (Nasdaq:AMMD) announced today early feedback from physicians on Perigee(TM), its innovative treatment for cystocele repair. Perigee is the most recent addition ...
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