SUI mesh

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FDA Rules To Reclassify POP Vaginal Mesh as High Risk!

Uphold, Boston Scientific, still on the market January 4, 2016 ~ An expert panel convened by the U.S. Food and Drug Administration (FDA) decided in September 2011 that mesh used to treat pelvic organ prolapse (POP) should be reclassified as high risk from its moderate risk (Class II) Read more

By | 2016-01-04T14:59:45+00:00 January 4th, 2016|News|42 Comments

FDA: Stress Urinary Incontinence (SUI) Surgical Mesh Reports up 36 Percent

March 29, 2013 ~ In September 2011, the U.S. Food and Drug Administration convened a panel of experts to try and get a handle on the concerning number of complications the agency was receiving about surgical mesh used to treat pelvic organ prolapse (POP)  and stress urinary incontinence (SUI).  The experts  Read more

By | 2013-03-29T01:17:24+00:00 March 29th, 2013|FDA News|13 Comments
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