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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 MANUFACTURING B.V. FEMORAL HEAD STERILE PRODUCT DO NOT REST 08/23/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_LINER 08/22/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SHELL 08/16/2023
STRYKER STRYKER CUP AND LINER 08/12/2023
ZIMMER BIOMET, INC. UNKNOWN HEAD 08/11/2023
ZIMMER BIOMET, INC. LINER STANDARD 3.5 MM OFFSET 36 MM I.D. 08/11/2023
ZIMMER BIOMET, INC. SHELL POROUS WITH CLUSTER HOLES 52 MM 08/11/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RIGHT HIP 07/31/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_STRYKER CUP 07/31/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_CORK_PRODUCT 07/25/2023
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