• 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 
 > 
 
44 records meeting your search criteria returned- Product Code: JWH Patient Problem: Myocardial Infarction Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNK KNEE FEMORAL SIGMA 03/04/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE TIBIAL INSERT SIGMA 03/04/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE TIBIAL TRAY SIGMA 03/04/2023
DEPUY ORTHOPAEDICS INC US PFC*SIGMA C/R NPOR FEM LT SZ5 01/18/2023
DEPUY ORTHOPAEDICS INC US PFC*SIGMA/OV/DOME PAT 3PEG,41 01/18/2023
DEPUY ORTHOPAEDICS INC US PFC*SIGMA/OV/DOME PAT 3PEG,41 01/17/2023
DEPUY ORTHOPAEDICS INC US PFC*SIGMA C/R NPOR FEM RT SZ 5 01/17/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE TIBIAL INSERT 04/21/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE TIBIAL TRAY 04/21/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL 04/21/2020
-
-