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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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8 records meeting your search criteria returned- Product Code: LZK Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
Unknown Manufacturer VITEK PROPLAST 11/13/2018
IMPLANTECH ASSOCIATES, INC. COMPOSITE¿ EPTFE-COATED FLOWERS DORSAL N 08/25/2017
IMPLANTECH ASSOCIATES, INC. FLOWERS EXTENDED TEAR TROUGH (R) IMPLANT 08/23/2017
IMPLANTECH ASSOCIATES, INC. CONFORM BINDER SUBMALAR (R) IMPLANT 10/27/2016
IMPLANTECH ASSOCIATES INC. FLOWERS TEAR THROUGH IMPLANT 09/10/2015
IMPLANTECH ASSOCIATES INC. COMBINED SUBMALAR SHELL IMPLANT 09/10/2015
IMPLANTECH ASSOCIATES CONFORM TERINO MALAR SHELL (R) 01/09/2015
IMPLANTECH ASSOCIATES, INC. TERINO MALAR SHELL IMPLANT 03/18/2014
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