Alcon Laboratories, Inc.

  • Manufacturer Address
    Alcon Laboratories, Inc., 15800 Alton Pkwy, Irvine CA 92618
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • 1 Event

One device in the database

  • Model / Serial
    Serial Numbers 0801438901X, 0801481701X2, 0801591601X2, 0801591701X1, 0801591801X1, 0801692701X1, 0801717801X3, 0801717901X, 0801718001X1, 0801718101X, 0801718201X, 0801763401X1, 0801763601X, 0801817201X, 0801817601X, 0801844601X1, 0801844701X1, 0801844801X1, 0801844901X, 0801845001X1, 0801887201X, 0801887501X, 0801887601X, 0801965801X, 0801965901X, 0801966001X, 0802057301X, 0802057501X, 0802244501X, 0802244701X, 0802245101X, 0802480501X, 0802480901X, 0802484101X, 0802514101X, 0802529501X, 0802570101X, 0801887401X, 0802244301X, 0801439201X, and 0802244901X,
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution --- USA including states of IL, WI, TX, MI, PA, NY, CT, SC, NC, LA, FL, GA, CA, OR, WA, CO, and NV, and countries of India, Bulgaria, Barbados, and Dominican Republic.
  • Product Description
    PurePoint System Operator's Manual, Catalog Number 8065751131, Rev. B for use with the Alcon PurePoint Laser, Catalog Number 8065750597 || Indicated for use in photocoagulation of both anterior and posterior segments of the eye.

14 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Alcon Laboratories, Inc., 2800 Discovery Dr., Orlando FL 32826
  • Source
    USFDA
  • Manufacturer Parent Company (2017)
  • Source
    AEMPSVFOI
  • Manufacturer Address
    Alcon, farmacevtske storitve, d.o.o. Verovškova ulica 57 1000 Ljubljana Slovenija Tel.: +386 (0)1 422 5280
  • Manufacturer Parent Company (2017)
  • Source
    AMPMDRS
9 more