• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
198 records meeting your search criteria returned- Product Code: OTO Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. GYNECARE GYNEMESH* PS 01/06/2016
ETHICON INC. GYNECARE GYNEMESH* PS 01/05/2016
ETHICON INC. GYNECARE GYNEMESH* PS 12/21/2015
COLOPLAST MANUFACTURING US, LLC RESTORELLE 11/23/2015
Unknown Manufacturer POLYPROPYLENE MESH 11/17/2015
ETHICON INC. ARTISYN Y-SHAPED MESH 11/17/2015
ETHICON INC. GYNECARE GYNEMESH 11/05/2015
ETHICON INC. GYNECARE GYNEMESH 11/03/2015
ETHICON INC. GYNECARE GYNEMESH 11/02/2015
ETHICON INC. GYNECARE GYNEMESH* PS 10/29/2015
-
-