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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: OTP Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 AVAULTA PLUS 06/11/2018
C. R. BARD AVAULTA PLUS BIOSYNTHETIC SUPPORT 05/16/2018
AMERICAN MEDICAL SYSTEMS INTEPRO Y-MESH 02/03/2016
COLOPLAST CORP EXAIR ANTERIOR 09/01/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYS 06/24/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYS 06/05/2015
ETHICON GYNECARE PROLIFT BLADDER SLING 03/30/2015
AMERICAN MEDICAL SYSTEMS (MN) UNKNOWN 03/24/2015
COLOPLAST A/S RESTORELLE DIRECT FIX POSTERIOR 01/11/2015
COLOPLAST A/S RESTORELLE DIRECT FIX POSTERIOR 01/11/2015
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