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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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39 records meeting your search criteria returned- Product Code: FBK Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
UNITED STATES ENDOSCOPY GROUP, INC. CARR-LOCKE INJECTION NEEDLE 01/27/2016
WILSON-COOK MEDICAL INC. GEL KIT 01/21/2015
C.R. BARD, INC. TEGRESS URETHRAL IMPLANT 10/31/2014
OLYMPUS MEDICAL SYSTEMS CORPORATION SINGLE USE INJECTOR 10/20/2014
WILSON-COOK MEDICAL INC GEL KIT 09/19/2014
C.R. BARD, INC. (COVINGTON) TEGRESS URETHRAL IMPLANT 09/17/2014
C.R. BARD, INC. (COVINGTON) TEGRESS URETHRAL IMPLANT 09/17/2014
WILSON-COOK MEDICAL INC GEL KIT 06/20/2014
BARD PUERTO RICO TEGRESS URETHRAL IMPLANT 06/18/2014
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