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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
ZIMMER GMBH UNKNOWN ALLOFIT CUP 11/27/2017
BIOMET UK LTD. UNKNOWN FEMORAL HEAD 11/23/2017
DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN DEPUY ASR ACETABULAR CUP 11/22/2017
DEPUY INTERNATIONAL LTD.8010379 DEPUY ASR XL FEM IMP SIZE 51 11/22/2017
DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN DEPUY STEM   11/22/2017
BIOMET UK LTD. UNKNOWN FEMORAL HEAD 11/22/2017
BIOMET UK LTD. UNKNOWN BI-METRIC STEM 11/22/2017
DEPUY INTERNATIONAL LTD. 8010379 TOTAL ASR FEM IMP SIZE 47 11/21/2017
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY STEM 11/21/2017
DEPUY INTERNATIONAL LTD. 8010379 DEPUY ASR XL FEM IMP SIZE 53 11/21/2017
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