• 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 
 > 
 
275 records meeting your search criteria returned- Product Code: JWH Product Problem: Loss of Osseointegration Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKN GENESIS II TOTAL KNEE PAT COMP 04/25/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® II MEDIAL PIVOT TIBIAL INSERT S 04/19/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® PRIMARY FEMORAL SIZE 3 RIGHT NO 04/19/2024
MICROPORT ORTHOPEDICS INC. EVOLUTION® NITRX? TIB KEELED 04/03/2024
STRYKER ORTHOPAEDICS-MAHWAH DURACON UNIVERSAL B/P NON-BEADED 03/02/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® POST STAB FEMORAL SIZE 2 NONPOR 01/23/2024
SMITH & NEPHEW, INC. GNS II POR FEM SIZE 6 LEFT 01/11/2024
SMITH & NEPHEW, INC. GNS II POROUS P/S FEM SZ4 RT 12/22/2023
MICROPORT ORTHOPEDICS INC. ADVANCE® ONLAY ALL-POLY PATELLA 38MM TRI 10/09/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SCORPIO NRG BASEPLATE 09/28/2023
-
-