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

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
375 records meeting your search criteria returned- Product Code: FTL Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ATRIUM MEDICAL CORPORATION C-QUR MESH 01/27/2017
COVIDIEN PARIETEX 12/28/2016
COLOPLAST A/S (2BO) RESTORELLE DIRECT FIX A 12/13/2016
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 12/06/2016
ATRIUM MEDICAL CORPORATION C-QUR MESH 12/06/2016
JOHNSON AND JOHNSON/ETHICON TVT BLADDER SLING 11/17/2016
BARD BARD PHARM. 11/08/2016
COLOPLAST A/S (2BO)RESTORELLE DIRECT FIX P 1 10/26/2016
COLOPLAST A/S (2BO)RESTORELLE DIRECTFIX POS 10/13/2016
COLOPLAST A/S RESTORELLE DIRECTFIX POS 09/27/2016
-
-