• 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
 

 
 
9 records meeting your search criteria returned- Product Code: JDG Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKNOWN FEMORAL HEAD MEMPHIS OXINIUM 05/29/2023
SMITH & NEPHEW, INC. ANTHOLOGY STARTER BROACH 11/30/2020
SMITH & NEPHEW, INC. ANTHOLOGY STARTER BROACH 11/30/2020
SMITH & NEPHEW, INC. ANTHOLOGY STARTER BROACH 11/30/2020
SMITH & NEPHEW, INC. ANTHOLOGY STD BROACH SIZE 1 09/08/2020
SMITH & NEPHEW, INC. ANTHOLOGY STD BROACH SIZE 1 09/08/2020
SMITH & NEPHEW, INC. ANTHOLOGY ANTERIOR BROACH HDLE KIT 09/07/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/04/2019
ZIMMER, INC. UNKNOWN FEMORAL HEAD 08/10/2017
-
-