Device Recall SoFlex SE Foldable Intraocular Lens

  • Modèle / numéro de série
    Model Number: LI61SE, Lot Number: 4916928.
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    Yes
  • Distribution
    Lenses were distributed to one distributor and 35 retailers. Worldwide Distribution -- Distributed to Canada, Taiwan and throughout the United States.
  • Description du dispositif
    Bausch & Lomb SoFlex SE Foldable Intraocular Lens. || UPC 4001404, Rx Only, STERILE. || Manufactured by: || Bausch & Lomb Incorporated, 21 Park Place Boulevard, Clearwater, FL 33759. || Intraocular lens indicated for primary implantation for visual correction in adult patients where the cataractous lens has been removed by phacoemulsification. The lens is intended for placement in the capsular bag.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Bausch & Lomb Inc, 1400 North Goodman Street, Rochester NY 14609-3547
  • Source
    USFDA