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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 
 
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
DEPUY ORTHOPAEDICS, INC. / JOHNSON & JOH DEPUY PINNACLE, WITH ULTAMET LINER 01/23/2019
DEPUY ORTHOPAEDICS, INC. 1818910 HIP HEAD 11/13 TAPER 28MM+0 01/21/2019
DEPUY ORTHOPAEDICS, INC. 1818910 SROM*STM ST,36+8L NK,18X13X160 01/18/2019
DEPUY ORTHOPAEDICS, INC. DEPUY 01/08/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP IMPLANT 01/02/2019
-
-