• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
18 records meeting your search criteria returned- Product Code: NJL Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US TRUMATCH CT CUT GUIDE KIT L 01/23/2024
DEPUY ORTHOPAEDICS INC US TRUMATCH CT CUT GUIDE KIT L 10/06/2023
DEPUY IRELAND - 9616671 TRUMATCH CT CUT GUIDE KIT L 03/16/2023
DEPUY ORTHOPAEDICS INC US TRUMATCH CT CUT GUIDE KIT R 04/25/2022
DEPUY ORTHOPAEDICS INC US TRUMATCH CT CUT GUIDE KIT L 03/11/2022
DEPUY ORTHOPAEDICS INC US TRUMATCH CT PIN GUIDE KIT R 07/28/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN PIN GUIDES 07/28/2021
DEPUY IRELAND - 9616671 ATTUNE CR RP INSRT SZ 6 5MM 12/26/2019
DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ 5 12MM 11/07/2019
DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 7 CEM 08/29/2019
-
-