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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Customed Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall Orthopedic Manual Surgical Instrument Orthopedic Devices Biomet, Inc. 1 United States USFDA
Device Recall MAKOplasty Hip Array Kit Laminate Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall RESTORIS PST Offset Shell Impactor Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Ossur Lil Angel Vest Orthopedic Devices Ossur H / F 1 United States USFDA
Device Recall Axial Torque Limiting Driver Orthopedic Devices Bradshaw Medical Inc. 1 United States USFDA