• 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 
 > 
 
47 records meeting your search criteria returned- Product Code: JDH Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. REF CUP POSITIONER/IMPACTOR 08/24/2018
SMITH & NEPHEW, INC. DYNOMITE 2.0 PK W/NDL,1#2-0 ULTRABRAID 07/12/2018
SMITH & NEPHEW, INC. TANDEM BIPOLAR COCR HEAD 05/08/2018
SMITH & NEPHEW, INC. SMITH AND NEPHEW HIP IMPLANT 02/09/2018
SMITH & NEPHEW, INC. SIZE 9 PRIMARY EMPERION STEM 03/23/2017
SMITH & NEPHEW, INC. TNDM BP SHL/XLPE LNR 41OD 26ID 10/25/2016
SMITH & NEPHEW, INC. OXINIUM FEMORAL HEAD 03/18/2016
SMITH & NEPHEW, INC. HIP IMPLANT PROSTHESIS 02/12/2016
SMITH & NEPHEW, INC. HIP IMPLANT PROSTHESIS 02/08/2016
SMITH & NEPHEW, INC. HIP IMPLANT 02/08/2016
-
-