• 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 
 > 
 
390 records meeting your search criteria returned- Product Code: JDI Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN HEAD 09/06/2023
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/+5 09/05/2023
MICROPORT ORTHOPEDICS INC. DYNASTY® BF SHELL PRIMARY 52MM GROUP D 09/04/2023
MICROPORT ORTHOPEDICS INC. PROFEMUR® NECK VAR/VAL 8DG LONG COBALT C 08/29/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN 28 +2.5 BIOLOX CERAMIC HEAD 08/25/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN LFIT V40 FEMORAL HEAD 08/24/2023
STRYKER ORTHOPAEDICS-MAHWAH 32MM +4 V40 TAPER VIT HEAD 08/24/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_36 +10 METAL HEAD 08/21/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_40 +4 METAL HEAD 07/25/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN HEAD 07/14/2023
-
-