• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
97 records meeting your search criteria returned- Product Code: NRA Product Problem: Device Slipped Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXFORD UNI TIBIAL TRAY SZ C LM PMA 02/27/2015
BIOMET UK LTD. OXFORD UNI FEMORAL MD 02/24/2015
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 4 PMA 02/12/2015
BIOMET UK LTD. OXF ANAT BRG RT LG SIZE 5 PMA 01/14/2015
BIOMET ORTHOPEDICS OXF UNI TIB TRAY SZ B RM PMA 01/06/2015
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 6 PMA 01/06/2015
BIOMET ORTHOPEDICS OXF UNI TIB TRAY SZA RM/LL PMA 11/24/2014
BIOMET ORTHOPEDICS UNKNOWN OXFORD KNEE 10/29/2014
BIOMET UK LTD. OXF UNI TIB TRAY SZ C RM PMA 10/02/2014
BIOMET UK LTD. OXFORD ANATOMIC BEARING LT SM SIZE 5 PMA 09/16/2014
-
-