Device Recall Silhouette Lift brochure

  • Modelo / Serial
    n/a.  This action does not involve recall or correction of any device. Only marketing materials are being considered in this action
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Distribution to the states of : CA, TX, IA, MA, RI, GA, WI, PA, VA, MO, FL, NE, MI, NY and CO., and Internationally to Canada.
  • Descripción del producto
    Silhouette Lift brochure || Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Silhouette Lift, Inc., 1 Technology Dr Ste F211, Irvine CA 92618-5336
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA