Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
125 records meeting your search criteria returned- Product Code: JDI Patient Problem: Swelling Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. TAPERLOC POR FMRL 17.5X155 07/29/2020
DEPUY INTERNATIONAL LTD - 8010379 ASR UNI FEMORAL IMPL SIZE 45 07/20/2020
DEPUY ORTHOPAEDICS INC US TC3 RP TIBIAL INSERT S4,20.0 06/29/2020
ZIMMER BIOMET, INC. UNKNOWN STEM 04/08/2020
DEPUY ORTHOPAEDICS INC US ARTICULEZE M HEAD 36MM +12 04/03/2020
DEPUY INTERNATIONAL LTD - 8010379 AML HIGH OFFSET LG STAT 15.0MM 04/01/2020
DEPUY ORTHOPAEDICS INC US ASPHERE M SPEC 12/14 44 +5 03/30/2020
BIOMET UK LTD. DELTA CER FM HD 036/0MM 12/14 03/23/2020
DEPUY ORTHOPAEDICS INC US 11/13 S-ROM 40MM M SPEC+6 03/09/2020
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 56MM 03/09/2020
-
-