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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 > 
 
60 records meeting your search criteria returned- Product Code: NRA Patient Problem: Swelling/ Edema Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF UNI TIB TRAY SZA LM 01/02/2024
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM SM PMA 01/02/2024
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 5 PMA 01/02/2024
BIOMET UK LTD. UNKNOWN TIBIA COMPONENT 12/18/2023
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 12/04/2023
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 12/04/2023
BIOMET UK LTD. UNKNOWN OXFORD BEARING 12/04/2023
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 6 PMA 10/05/2023
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM SM PMA 10/05/2023
BIOMET UK LTD. OXF UNI TIB TRAY SZA RM 10/05/2023
-
-