• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF UNI CMNTLS TIB SZ C RM 08/29/2023
BIOMET UK LTD. OXF TWIN PEG CMNTLS FMRL MD 08/29/2023
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 3 PMA 08/29/2023
BIOMET UK LTD. OXF ANAT BRG RT SM SIZE 4 PMA 08/17/2023
BIOMET UK LTD. OXF UNI TIB TRAY SZ AA RM PMA 08/17/2023
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM SM PMA 08/17/2023
BIOMET, INC. TIBIAL INSERT 08/15/2023
BIOMET, INC. TIBIAL TRAY 08/15/2023
BIOMET, INC. FEMORAL COMPONENT 08/15/2023
BIOMET UK LTD. UNKNOWN BIOMET OXFORD TIBIAL TRAY 07/28/2023
-
-