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
 

 
 
7 records meeting your search criteria returned- Product Code: LNM Patient Problem: Swelling Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
UROPLASTIQUE MACROPLASTIQUE IMPLANT 10/20/2016
UROPLASTIQUE MACROPLASTIQUE IMPLANT 10/20/2016
C.R. BARD, INC. (COVINGTON) -1018233 CONTIGEN® BARD® COLLAGEN IMPLANT 06/14/2016
C.R. BARD, INC. (COVINGTON) -1018233 CONTIGEN BARD COLLAGEN IMPLANT 11/17/2015
MERZ NORTH AMERICA, INC. COAPTITE INJECTABLE IMPLANT 10/29/2014
MERZ NORTH AMERICA, INC. COAPTITE INJECTABLE IMPLANT 10/29/2014
SALIX PHARMACEUTICAL SOLESTA 50MG/ML 02/18/2014
-
-