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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
SMITH & NEPHEW, INC. LGN OFFSET COUPLER TRIAL 6MM 02/02/2020
MICROPORT ORTHOPEDICS INC. INSERT 01/29/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 7 STANDARD 1 01/28/2020
BIOMET UK LTD. UNK OXFORD BEARING 01/27/2020
ZIMMER BIOMET, INC. SERIES A PAT STD 31 3 PEG 01/22/2020
BIOMET UK LTD. EXCEED ABT 3HL SHELL 44/54MM 01/16/2020
ENCORE MEDICAL L.P. UNI KNEE 01/10/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 5 STANDARD 1 01/10/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 6 STANDARD 1 01/06/2020
MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 4 STANDARD 1 01/03/2020
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