• 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 
 6 
 7 
 8 
 9 
 > 
 
82 records meeting your search criteria returned- Product Code: JDH Report Date From: 1/1/2017 Report Date To: 12/31/2017

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. R3 0DEG 32MM TRIAL 50MM 11/14/2017
SMITH & NEPHEW, INC. HIP IMPLANT 11/10/2017
SMITH & NEPHEW, INC. HIP IMPLANT 11/08/2017
SMITH & NEPHEW, INC. R3 42MM ID US COCR LNR 54MM 11/07/2017
SMITH & NEPHEW, INC. TBD 10/23/2017
SMITH & NEPHEW, INC. M-COR FEMORAL NECK 10/18/2017
SMITH & NEPHEW, INC. SMITH AND NEPHEW HIP IMPLANT 10/13/2017
SMITH & NEPHEW, INC. UNKNOWN OXINIUM HEAD 09/25/2017
SMITH & NEPHEW, INC. UNKNOWN ECHELON STEM 09/25/2017
SMITH & NEPHEW, INC. UNKNOWN R3 LINER 09/25/2017
-
-