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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
105 records meeting your search criteria returned- Product Code: NRA Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNKNOWN OXFORD BEARING 01/13/2020
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 01/13/2020
BIOMET UK LTD. OXFORD UNI TWIN-PEG FEMORAL SM 01/10/2020
BIOMET UK LTD. OXF ANAT BRG RT SM SIZE 3 PMA 01/08/2020
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 01/08/2020
BIOMET UK LTD. UNKNOWN OXFORD BEARING 01/08/2020
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 01/08/2020
BIOMET UK LTD. OXF UNI PH3 TIB IMPACTOR 11/01/2019
BIOMET UK LTD. OXF CMNTLS IMPLANT INSERT IMPACTOR 10/29/2019
BIOMET UK LTD. OXFORD UNI TIB BRG LG SZ3 10/29/2019
-
-