• 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 
 3 
 4 
 > 
 
35 records meeting your search criteria returned- Product Code: KWS Product Problem: Device-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 XTND 145 RSA REAM GUID INSRTR 09/19/2022
DEPUY IRELAND - 9616671 XTND 145 RSA REAM GUID INSRTR 01/17/2022
TORNIER S.A.S. AEQ REV II GLENOID BASEPLATEDIA 25 MM 12/29/2021
DEPUY IRELAND - 9616671 XTND 145 RSA REAM GUID INSRTR 04/12/2021
DEPUY IRELAND - 9616671 XTND 145 RSA REAM GUID INSRTR 01/05/2021
TORNIER INC AEQUALIS FLEX REVIVE SHOULDER SYSTEM 11/04/2020
ARTHREX, INC. VIP GLENOID 3D MODEL 10/23/2020
STANMORE IMPLANTS WORLDWIDE UNKNOWN METS BAYLEY/WALKER DEVICE 08/24/2020
DEPUY FRANCE SAS - 3003895575 DXTEND SCREW LOCK D4.5X42MM 07/13/2020
DEPUY FRANCE SAS - 3003895575 DXTEND METAGLENE 04/01/2020
-
-