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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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375 records meeting your search criteria returned- Product Code: FTL Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES UNKNOWN 09/26/2016
ETHICON GYNCARE MESH 09/12/2016
COLOPLAST A/S RESTORELLE DIRECTFIX ANTEIOR 08/25/2016
ETHICON PROLENE MESH WITH PLUG 08/18/2016
COLOPLAST A/S UNKNOWN FEM PELVIC HEALTH MESH 08/15/2016
ETHICON AW PROCEED SURGICAL MESH 08/14/2016
W.L. GORE & ASSOCIATES GORE DUALMESH® BIOMATERIAL 07/15/2016
BARD MONOFILAMENT KNITTED POLYPROPYLENE MESH 07/09/2016
ETHICON PHYSIOMESH FLEXIBLE COMPOSITE MESH 06/23/2016
ETHICON PHYSIOMESH FLEXIBLE COMPOSITE MESH 06/23/2016
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