• 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 
 > 
 
44 records meeting your search criteria returned- Product Code: KWY Patient Problem: Synovitis Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY METAL FEMORAL HEAD 01/12/2017
DEPUY ORTHOPAEDICS, INC. UNK DEPUY FEMORAL STEM 12/27/2016
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY FEMORAL STEM 11/10/2016
DEPUY ORTHOPAEDICS INC US UNKNOWN DEPUY METAL FEMORAL HEAD 11/10/2016
DEPUY IRELAND - 9616671 S-ROM*SLEEVE PRX ZTT, 18F-LRG 08/15/2016
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY STEM 06/02/2016
BIOMET ORTHOPEDICS M2A TPR HI CARBON 41/32MM LNR 05/06/2016
BIOMET ORTHOPEDICS 32MM M2A HI CARBON HD +3MM NK 05/06/2016
DEPUY INTL.,LTD 8010379 UNIDENTIFIED ASR TAPER SLEEVE 12/23/2015
AESCULAP IMPLANT SYSTEMS, LLC, A DIV OF TOTAL HIP REPLACEMENT SYSTEM 12/16/2015
-
-