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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
EXACTECH, INC. SPECIFIC DEVICE NOT REPORTED 01/22/2024
EXACTECH, INC. NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CU 01/18/2024
EXACTECH, INC. COCR FEM HEAD 36MM +0 OFFSET 12/14 01/11/2024
EXACTECH, INC. WEDGE PLASMA X/O SZ 12 01/11/2024
EXACTECH, INC. NV GXL LNR, +5LAT, 32MM G1-48/50MM CUPS 01/09/2024
EXACTECH, INC. NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS 01/07/2024
CORIN LTD TAPERFIT 01/05/2024
EXACTECH, INC. HIP COMPONENTS 01/02/2024
MICROPORT ORTHOPEDICS INC. UNKNOW ADVANCE MEDIAL PIVOT SYSTEM 12/28/2023
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM 0 OFFSET 12/20/2023
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