• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
143 records meeting your search criteria returned- Product Code: FSM Product Problem: Contamination /Decontamination Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US STERILIZATION CASE 7IN 08/24/2020
DEPUY ORTHOPAEDICS INC US PINN TRIAL LINER TRAY 48-66 08/17/2020
DEPUY ORTHOPAEDICS INC US PINN INST CASE W/TRAY AND LID 08/17/2020
DEPUY ORTHOPAEDICS INC US TRIAL SHELL TRAY 47/48-65/66 08/17/2020
DEPUY ORTHOPAEDICS INC US PINN IMPACTION INST TRAY 08/17/2020
DEPUY ORTHOPAEDICS INC US UNK INSTRUMENT CASE 02/12/2020
DEPUY IRELAND - 9616671 ATTUNE REV GEN FEM PREP CASE 11/06/2019
DEPUY ORTHOPAEDICS INC US TISSUE SPARING FEM CORE CASE 1 10/22/2019
DEPUY ORTHOPAEDICS INC US TISSUE SPARING FEM CORE CASE 1 10/22/2019
DEPUY IRELAND - 9616671 SIG HP REV FEMORAL PREP CASE 09/18/2019
-
-