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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 03/11/2020
BIOMET UK LTD. UNKNOWN OXFORD BEARING 03/11/2020
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 03/11/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 4 STANDARD 1 03/11/2020
MICROPORT ORTHOPEDICS INC. FEMORAL HEAD BIOLOX DELTA CERAMIC 12/14 02/18/2020
BIOMET UK LTD. UNKNOWN OXFORD BEARING 02/12/2020
ZIMMER BIOMET, INC. SERIES A PATELLA STD 02/04/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP FEM CS/CR NONPOROUS 02/03/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION TIB KEELED NONPOROUS 02/03/2020
SMITH & NEPHEW, INC. LGN OFFSET COUPLER TRIAL 6MM 02/02/2020
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