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
 

 
 
9 records meeting your search criteria returned- Product Code: NRA Product Problem: Tear, Rip or Hole in Device Packaging 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 SZ D LM PMA 02/26/2024
BIOMET UK LTD. OXF UNI TIB TRAY SZ AA RM PMA 06/30/2021
BIOMET UK LTD. TINBN VG INT PS ANAT FM L 70MM 70 MM 10/02/2019
BIOMET UK LTD. OXF TWIN-PEG CMNTD FEM XS PMA 05/09/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ C RM PMA 04/09/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ B LM PMA 02/25/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ D RM PMA 02/19/2019
BIOMET UK LTD. OXF UNI TIB TRAY SZ F RM PMA 10/10/2017
BIOMET UK LTD. OXFORD UNICOMPARTMENTAL KNEE CEMENTLESS 10/21/2016
-
-