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

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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
213 records meeting your search criteria returned- Product Code: NRA Patient Problem: Unspecified Infection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF PKS ANAT MEN BRG UHMWPE RT LRG SZ 3 02/10/2016
BIOMET UK LTD. OXF PKS ANAT MEN BEARING UHMWPE RT LRG S 02/09/2016
BIOMET UK LTD. OXF UNI C/LESS TIB TRAY RM E 02/09/2016
BIOMET UK LTD. OXFORD PH3 CEMENTLESS FEM SZ L 02/09/2016
BIOMET UK LTD. OXF PKS ANAT MEN BRG UHMWPE LT SML SZ 3 01/21/2016
BIOMET UK LTD. OXF PKS ANAT MEN BEARING UHMWPE RT MED S 12/18/2015
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 3 PMA 11/12/2015
BIOMET ORTHOPEDICS UNKNOWN KNEE 09/22/2015
BIOMET UK LTD. OXFORD BEARING 09/03/2015
BIOMET UK LTD. OXF PKS ANAT MEN BEARING UHMWPE LT SML S 09/01/2015
-
-