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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 BIOMET, INC. UNK HEAD 05/07/2024
ZIMMER BIOMET, INC. UNK LINER 05/07/2024
DEPUY ORTHOPAEDICS INC US ALTRX NEUT 36IDX56OD 05/07/2024
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN RESTORATION MODULAR DISTAL STEM 05/07/2024
STRYKER ORTHOPAEDICS-MAHWAH RT FLANGED ACET CUP SIZE E TRIDENT ID 05/07/2024
DEPUY ORTHOPAEDICS INC US UNK HIP FEMORAL STEM SUMMIT 05/06/2024
FINSBURY ORTHOPAEDICS LIMITED UNKNOWN HIP ACETABULAR CUP 05/06/2024
ZIMMER BIOMET, INC. FEMORAL HEAD STERILE PRODUCT DO NOT REST 05/06/2024
DEPUY ORTHOPAEDICS INC US ALTRX NEUT 32IDX52OD 05/06/2024
ZIMMER BIOMET, INC. XLPE 10DEG POLY LINER 64 X 40 05/06/2024
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