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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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110 records meeting your search criteria returned- Product Code: JDL Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. LINEAGE TRANSCEND METAL ACETABULAR LINER 02/09/2021
ZIMMER MANUFACTURING B.V. COCR FEMORAL HEAD 10/27/2019
ZIMMER BIOMET, INC. 32MM MOD HEAD COCR -3MM NECK 08/29/2019
DEPUY ORTHOPAEDICS INC US 5.0MM DIA TPRD HD PER SCRW 65 12/14/2018
DEPUY ORTHOPAEDICS INC US 5.0MM DIA TPRD HD PER SCRW 65 12/14/2018
ZIMMER GMBH UNKNOWN FITMORE STEM 08/08/2018
ZIMMER BIOMET, INC. UNKNOWN CUP 11/20/2017
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS HEAD 02/09/2016
MICROPORT ORTHOPEDICS INC. CONSERVE(R) TOTAL A-CLASS(R) FEMORAL HEA 02/04/2016
MICROPORT ORTHOPEDICS INC. CONSERVE HEAD 02/04/2016
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