• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
99 records meeting your search criteria returned- Product Code: JDI Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EXACTECH, INC. EXACTECH ACETABULAR LINER 11/10/2014
EXACTECH, INC. EXACTECH FEMORAL HEAD 11/10/2014
ZIMMER GMBH unknown brand name 11/07/2014
SMITH & NEPHEW BIRMINGHAM HIP RESURFACE 10/30/2014
BIOMET ORTHOPEDICS TAPERLOC POR FMRL LAT 13.5X147 10/30/2014
BIOMET ORTHOPEDICS 28MM DIA COCR MODULAR HEAD -6MM NK 10/22/2014
ZIMMER GMBH WINTERTHUR HIPS 10/21/2014
STRYKER IRELAND, LTD. OSTEONICS (ORTHOPA LRG TAP PRI MOD NCK 0DEG 34MM 10/21/2014
ZIMMER GMBH CLS STEM 145 9.0 12 14 10/16/2014
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/+5 09/30/2014
-
-