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

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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
106 records meeting your search criteria returned- Product Code: MDM 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
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 08/27/2018
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 08/22/2018
SMITH AND NEPHEW, INC. FEMORAL IMPLANT IMPACTOR 08/21/2018
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 08/20/2018
ARTHREX, INC. DISPS KIT,TRANS-TIB ACL W/O SAWBLD 08/14/2018
ETHICON ENDO-SURGERY, LLC. ENDOPATH*BLUNT CHERRY DISSECT 08/01/2018
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 07/16/2018
ETHICON ENDO-SURGERY, LLC. ENDOPATH*BLUNT CHERRY DISSECT 07/06/2018
ETHICON ENDO-SURGERY, LLC. ENDOPATH*BLUNT CHERRY DISSECT 07/06/2018
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 12/15/2015
-
-