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

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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
123 records meeting your search criteria returned- Product Code: LRN Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OBERDORF SYNTHES PRODUKTIONS GMBH WIRE, SURGICAL 02/19/2019
OBERDORF SYNTHES PRODUKTIONS GMBH 1.25MM THREADED GUIDE WIRE 150MM 02/12/2019
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 01/03/2019
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE,SURGICAL 08/13/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 06/11/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 06/11/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 04/24/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 03/27/2018
OBERDORF : SYNTHES PRODUKTIONS GMBH WIRE, SURGICAL 01/25/2018
WRIGHTS LANE: SYNTHES USA PRODUCTS LLC WIRE, SURGICAL 12/15/2017
-
-