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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
325 records meeting your search criteria returned- Product Code: JWH Product Problem: Material Integrity Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. PROFIX ZIRCON OX NP FEM SZ5 LT 07/06/2017
MAKO SURGICAL CORP. UNKNOWN PKA INSERT TRIALS 06/22/2017
STRYKER ORTHOPAEDICS-MAHWAH NRG KNEE P/S NRG BEARING INSERT SIZE 05/22/2017
STRYKER ORTHOPAEDICS-MAHWAH SCORPIO-FLEX PS X3 TIB INSERT 04/05/2017
STRYKER ORTHOPAEDICS-MAHWAH SCORPIO-FLEX PS X3 TIB INSERT 03/29/2017
STRYKER ORTHOPAEDICS-MAHWAH PS TIBIAL INSERT TRIAL #5 - 11MM 03/29/2017
STRYKER ORTHOPAEDICS-MAHWAH SCORPIO C-DOME PATELLA 03/24/2017
STRYKER ORTHOPAEDICS-MAHWAH CR TIBIAL INSERT TRIAL #4 - 13MM 03/06/2017
STRYKER ORTHOPAEDICS-MAHWAH PS TIBIAL INSERT TRIAL #4 - 16MM 03/02/2017
STRYKER ORTHOPAEDICS-MAHWAH SCORPIO NRG X3 PS TIBIAL INSERT #9 10MM 02/15/2017
-
-