• 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 
 
 
11 records meeting your search criteria returned- Product Code: LWJ Product Problem: Migration Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG BIPOLAR CUP ID28MM OD51MM SELF-CENTERING 08/02/2021
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. MODULAR-PLUS REVISION STEM (UNKN. 06/02/2021
AESCULAP AG ISODUR PROSTHESIS HEAD 8/10 28MM L 05/13/2021
AESCULAP AG ISODUR PROSTHESIS HEAD 8/10 28MM M 05/13/2021
DEPUY ORTHOPAEDICS INC US SROM*STM ST,30+4L NK,16X11X150 05/04/2021
DEPUY ORTHOPAEDICS INC US SUMMIT BASIC PRESS FIT SZ 4 02/01/2021
DEPUY IRELAND 9616671 CORAIL REVISION STEM HO 14 01/06/2021
AESCULAP AG ISODUR PROSTHESIS HEAD 8/10 22.2MM M 03/10/2020
AESCULAP AG COLLECT.NO.QAS FEM.HEADS BIOLOX 03/04/2020
AESCULAP AG COLLECT.NO.QAS FEM.HEADS BIOLOX 03/04/2020
-
-