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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
252 records meeting your search criteria returned- Product Code: NRA Report Date From: 1/1/2018 Report Date To: 12/31/2018

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF TWIN PEG CMNTLS FMRL MD 08/02/2018
BIOMET UK LTD. OXF TWIN PEG CMNTLS FMRL LG 06/28/2018
BIOMET UK LTD. OXFORD CEMENTLESS TIBIA E LM 06/28/2018
BIOMET UK LTD. OXFORD UNI FEMORAL SM 06/20/2018
ZIMMER BIOMET, INC. UNKNOWN OXFORD KNEE PROSTHESIS 06/16/2018
BIOMET UK LTD. OXFORD CEMENTLESS TIBIA C LM 06/14/2018
ZIMMER BIOMET, INC. OXFORD TRIAL BEARING SM SZ 4/5 06/05/2018
BIOMET UK LTD. OXF UNI TIB TRAY SZ C RM PMA 05/23/2018
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 4 PMA 05/23/2018
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM MD PMA 05/23/2018
-
-