• 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 
 > 
 
214 records meeting your search criteria returned- Product Code: JWH Patient Problem: Impaired Healing Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TIBIAL TRAY 12/08/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TIBIAL INSERT 12/08/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN ANKLE TALAR 12/08/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE FEMORAL SIGMA 11/09/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE PATELLA SIGMA 11/09/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE TIBIAL INSERT SIGMA 11/09/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE TIBIAL TRAY SIGMA 11/09/2023
ZIMMER BIOMET, INC. UNKNOWN CEMENT 11/09/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL 08/21/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE TIBIAL TRAY 08/21/2023
-
-