• 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 
 > 
 
74 records meeting your search criteria returned- Product Code: NRA Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM MD PMA 06/07/2023
BIOMET UK LTD. OXF UNI CMNTLS TIB SZ C LM 06/01/2023
BIOMET UK LTD. OXF TRL BRG W/SLOTS LGE 3MM 04/27/2023
BIOMET UK LTD. OXFORD PKS ANATOMIC ARCOM MENISCAL BRG - 04/19/2023
BIOMET UK LTD. OXF UNI TIB TRAY SZ C RM PMA 02/13/2023
BIOMET UK LTD. OXF ANAT BRG RT LG SIZE 4 PMA 02/13/2023
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM LG PMA 01/25/2023
BIOMET UK LTD. OXF CMNTLS IMPLANT INSERT 01/03/2023
BIOMET UK LTD. OXFORD PKS CEMENTED TIBIA, ALPHA, STANDA 12/28/2022
BIOMET UK LTD. OXF ANAT BRG LT SM SIZE 5 PMA 12/20/2022
-
-