Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
6 records meeting your search criteria returned- Product Code: KWA Product Problem: Fluid/Blood Leak Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER GMBH DUROM ACETABULAR COMPONENT 46/40 F 05/26/2016
ZIMMER GMBH DUROM ACETABULAR COMPONENT 50/44 J 04/26/2016
ZIMMER GMBH DUROM ACETABULAR COMPONENT 48/42 H 04/22/2016
BIOMET ORTHOPEDICS M2A-MAGNUM MOD HD SZ 48MM 06/10/2015
BIOMET ORTHOPEDICS M2A-MAGNUM MOD HD SZ 46MM 06/10/2015
BIOMET ORTHOPEDICS SELEX/MAGNUM MOD HD 40MM -6 04/20/2015
-
-