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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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4 records meeting your search criteria returned- Product Code: LNM Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 CONTIGEN BARD COLLAGEN IMPLANT 10/20/2015
SALIX PHARMACEUTICALS, INC SOLESTA 09/15/2015
MERZ NORTH AMERICA, INC. COAPTITE INJECTABLE IMPLANT 04/27/2015
Unknown Manufacturer SOLESTA 50MG/ML 08/05/2014
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