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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 
 
80 records meeting your search criteria returned- Product Code: MDM Product Problem: Entrapment of Device Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 02/17/2017
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 12/29/2016
SMITH & NEPHEW, INC. 2.0/2.7MM DRILL GUIDE 09/28/2016
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 02/23/2016
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 12/15/2015
SMITH & NEPHEW, INC. INTERTAN INSTRUMENTS 02/18/2015
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 05/13/2014
ARTHREX, INC. FLIPCUTTER II, SHORT 10MM 04/25/2014
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 02/27/2014
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 02/13/2014
-
-