• 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 
 10 
 > 
 
251 records meeting your search criteria returned- Product Code: JWH Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. PERSONA POSTERIOR REFERENCING SERIES 1 S 04/26/2024
ZIMMER BIOMET, INC. UNKNOWN BEARING 04/22/2024
ZIMMER ORTHOPAEDIC MFG. LTD. PERSONA TIBIA CEMENTED STEMMED 04/15/2024
ZIMMER BIOMET, INC. UNKNOWN ARTICULAR SURFACE 04/04/2024
SMITH & NEPHEW, INC. VIS ADPT GUIDE LGNP FEM 04/02/2024
SMITH & NEPHEW, INC. GNS II CMT TIB SIZE 4 LEFT 04/01/2024
SMITH & NEPHEW, INC. VIS ADPT GUIDE LGNP KIT 03/18/2024
ZIMMER ORTHOPAEDIC MFG. LTD. PERSONA TIBIA CEMENTED 5 DEGREE STEMMED 03/12/2024
SMITH & NEPHEW, INC. NS VIS ADPT GUIDE JII KIT 02/23/2024
SMITH & NEPHEW, INC. NS VIS ADPT GUIDE JII KIT 02/12/2024
-
-