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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 STEM 11/29/2023
STRYKER ORTHOPAEDICS-MAHWAH SIZE 5 ACCOLADE II 127 DEG 11/28/2023
STRYKER ORTHOPAEDICS-MAHWAH ACCOLADE (127 DEG) SIZE 2.5 ACCOLADE ( 11/10/2023
ZIMMER MANUFACTURING B.V. FEMORAL HEAD STERILE PRODUCT DO NOT REST 11/09/2023
ZIMMER BIOMET, INC. UNKNOWN STEM 11/09/2023
ZIMMER BIOMET, INC. M2A-MAGNUM PF CUP 50ODX44ID 11/08/2023
STRYKER ORTHOPAEDICS-MAHWAH ACCOLADE (127 DEG) SIZE 3.5 ACCOLADE ( 11/07/2023
STRYKER ORTHOPAEDICS-MAHWAH SIZE 6 ACCOLADE II 127 DEG 11/04/2023
STRYKER ORTHOPAEDICS-MAHWAH ACCOLADE 132 SIZE 3.5 11/02/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_HIP 10/26/2023
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