Devices

Device Recall Silhouette Lift brochure

  • Modèle / numéro de série
    n/a.  This action does not involve recall or correction of any device. Only marketing materials are being considered in this action
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    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.
  • Description du dispositif
    Silhouette Lift brochure || Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.
  • Manufacturer
    Silhouette Lift, Inc.
  • 1 Event

Fabricant

Silhouette Lift, Inc.
  • Adresse du fabricant
    Silhouette Lift, Inc., 1 Technology Dr Ste F211, Irvine CA 92618-5336
  • Société-mère du fabricant (2017)
    Silhouette Lift Inc.
  • Source
    USFDA