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
 

 
 < 
 1 
 2 
 3 
 > 
 
25 records meeting your search criteria returned- Product Code: NQP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER SWITZERLAND MANUFACTURING GMBH DYNESYS LIS, STABILIZING CORD, 200 09/14/2020
ZIMMER GMBH UNKNOWN DYNESYS SPINE IMPLANT 05/21/2019
SYNTHES USA ROD 09/21/2017
SYNTHES USA ROD 09/21/2017
ZIMMER GMBH DYNESYS LIS, STABILIZING CORD, 100 05/29/2017
ZIMMER GMBH DYNESYS, UNIVERSAL SPACER, 6-45 04/11/2017
ZIMMER GMBH UNKNOWN DYNESYS SPINE IMPLANT 02/08/2017
ZIMMER GMBH UNKNOWN DYNESYS SPINE IMPLANT 02/08/2017
ZIMMER GMBH UNKNOWN DYNESYS SPINE IMPLANT 02/08/2017
ZIMMER GMBH UNKNOWN DYNESYS IMPLANT 12/02/2016
-
-