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
 

 
 
9 records meeting your search criteria returned- Product Code: LWJ Patient Problem: Death Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG PLASMACUP SC SIZE 52MM 05/02/2019
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 32MM L 05/02/2019
AESCULAP AG PLASMAFIT PLUS 3 CUP SIZE 56MM I 05/02/2019
AESCULAP AG SC/MSC CERAMICS INSERT 32MM 52/54 SYM. 05/02/2019
STRYKER ORTHOPAEDICS-MAHWAH C-TAPER COCR LFIT HEAD 26MM/+10 09/12/2018
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 04/05/2018
ZIMMER BIOMET, INC. UNKNOWN HIP 10/17/2017
DEPUY IRELAND 9616671 SROM*STM ST,36+8L NK,24X19X175 06/29/2016
BIOMET ORTHOPEDICS UNKNOWN HIP 03/09/2016
-
-