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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 10 
 > 
 
311 records meeting your search criteria returned- Product Code: JWH Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. VIS ADPT GUIDE KIT JII 12/06/2022
SMITH & NEPHEW, INC. UNKNOWN ORTHOPAEDIC RECONSTRUCTION DEV 12/06/2022
SMITH & NEPHEW, INC. VIS ADPT GUIDE LGNP KIT 11/14/2022
SMITH & NEPHEW, INC. LEGION CR OXIN FEM SZ7 LT 11/11/2022
SMITH & NEPHEW, INC. VIS ADPT GUIDE LGNP KIT 11/05/2022
SMITH & NEPHEW, INC. NS VIS ADPT GUIDE JII KIT 11/01/2022
SMITH & NEPHEW, INC. NS VIS UK MED KIT 10/26/2022
EXACTECH, INC. TRULIANT TIB IMP PS INSERT SZ 2.5 11MM 08/19/2022
SMITH & NEPHEW, INC. VIS ADPT GUIDE KIT JII 08/03/2022
ZIMMER BIOMET, INC. UNKNOWN TIBIAL BEARING 08/02/2022
-
-