• 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
 

 
 < 
 1 
 2 
 3 
 4 
 > 
 
33 records meeting your search criteria returned- Product Code: OTM Patient Problem: Urinary Retention Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AMERICAN MEDICAL SYSTEMS, INC. UNKNOWN GRAFT MESH 07/15/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 07/15/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 06/23/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 01/27/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 10/17/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 09/30/2014
COLOPLAST A/S VIRTUE ONE SLING 09/24/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 08/18/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 07/14/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ADVANCE MALE SLING SYSTEM 07/01/2014
-
-