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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
ENCORE MEDICAL L.P EMPOWR PS KNEETM FEMUR, NONPOROUS, 9L 04/14/2023
ENCORE MEDICAL L.P 242-01-105 04/14/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SCORPIO-FLEX PS INSERT 04/11/2023
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN SCORPIO-FLEX PATELLAR COMPONENT 04/11/2023
ZIMMER BIOMET, INC. UNKNOWN NEXGEN TIBIAL TRAY 04/11/2023
ZIMMER BIOMET, INC. UNKNOWN NEXGEN ARTICULAR SURFACE 04/11/2023
ZIMMER BIOMET, INC. UNKNOWN NEXGEN FEMORAL 04/11/2023
ZIMMER BIOMET, INC. UNK NEXGEN ARTICULAR SURFACE 04/11/2023
ZIMMER BIOMET, INC. UNK NEXGEN TIBIAL 04/11/2023
ZIMMER BIOMET, INC. UNK NEXGEN FEMORAL 04/11/2023
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