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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. E1 VNGD AS TIB BRG 12X67 05/09/2023
ZIMMER BIOMET, INC. VANGUARD CR ILOK FEM-LT 62.5 05/09/2023
ZIMMER BIOMET, INC. SERIES A PAT STD 31 3 PEG 05/09/2023
ZIMMER BIOMET, INC. BIOMET CC CRUCIATE TRAY 67MM 05/09/2023
ZIMMER BIOMET, INC. UNK NEXGEN ARTICULAR SURFACE 04/11/2023
ZIMMER BIOMET, INC. UNK NEXGEN TIBIAL 04/11/2023
ZIMMER BIOMET, INC. UNK NEXGEN FEMORAL 04/11/2023
DEPUY ORTHOPAEDICS INC US UNK KNEE FEMORAL SIGMA 03/23/2023
DEPUY IRELAND - 9616671 ATTUNE FB TIB BASE SZ 3 CEM 03/20/2023
ZIMMER BIOMET, INC. ARTICULAR SURFACE FIXED BEARING CONSTRAI 11/28/2022
-
-