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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. UNKNOWN RINGLOC CUP 04/26/2023
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL STEM 04/19/2023
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ6 HI OFF 04/13/2023
DEPUY ORTHOPAEDICS INC US 12/14 ARTICUL 40MM M SPEC+8.5 04/13/2023
ZIMMER BIOMET, INC. UNKNOWN FEMORAL HEAD 04/13/2023
ZIMMER BIOMET, INC. UNKNOWN LINER 04/13/2023
DEPUY ORTHOPAEDICS INC US ALTRX NEUT 36IDX54OD 04/11/2023
DEPUY ORTHOPAEDICS INC US UNK ATTUNE FEMORAL 03/23/2023
STRYKER ORTHOPAEDICS-MAHWAH C-TAPER COCR LFIT HEAD 36MM/+5 03/22/2023
DEPUY ORTHOPAEDICS INC US UNK HIP ACETABULAR CUP PINNACLE 03/17/2023
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