Giving an elegant OZil® performance with
accelerated cataract removal,*,1 enhanced
torsional efficiency1,2 and reduced repulsion.3





*As compared to the INFINITI® Vision System,
bottle gravity system. 


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The Centurion® Vision System was designed to set the global standard for efficiency in the OR. The system features the unique combination of OZil® technology and innovative fluidics for enhanced emulsification that requires minimal fluid.

Cumulative Dissipated Energy

Chart showing the energy used with CENTURION<sup>®</sup> Vision System and that 39 percent was reduced compared to INFINITI<sup>®</sup> Vision System.

Group difference (95% confidence interval): -2.78 (-3.44 to -2.13) percent-seconds; data reflect least squares mean ± standard error.

Aspiration Fluid Used

Chart showing the fluid used with CENTURION® Vision System and that 14 percent was reduced compared to INFINITI® Vision System.

Group difference (95% confidence interval): -6.12 (-9.82 to -2.43) mL; data reflect least squares mean ± standard error.

Aspiration Time

Group difference (95% confidence interval): -15.78 (-26.49 to -5.07) seconds; data reflect least squares mean ± standard error.

INFINITI® Configuration: INFINITI® Vision System, 45° Mini Flared Kelman with Ultra Sleeve

Centurion® Configuration: Centurion® Vision System, 45° BALANCED Tip with INTREPID® Ultra Sleeve

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Designed to enhance surgeon
control during IOL insertions with
a micro-incisional portfolio

Surgical Experience

Surgical Experience

Smooth, responsive and efficient
performance through superior

  1. Solomon K, Lorente R, Cionni R, Fanney D. Prospective, randomized clinical study using a new phaco system with intraocular system target pressure control. ASCRS-ASOA Symposium and Congress; April 25-29, 2014; Boston, USA.
  2. Zacharias J. Comparative motion profile characterization of the mini flared and balanced phacoemulsification tips. ESCRS; September 5-9, 2015; Barcelona, Spain.
  3. Vasavada AR, et al. Comparison of torsional and microburst longitudinal phacoemulsification: a prospective, randomized, masked clinical trial. Ophthalmic Surg Lasers Imaging. 2010;41(1):109-114.

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CAUTION: Federal (USA) law restricts this device to sale by, or on the order of, a physician.

As part of a properly maintained surgical environment, it is recommended that a backup IOL Injector be made available in the event the AutoSert® IOL Injector Handpiece does not perform as expected.

INDICATION: The Centurion® Vision System is indicated for emulsification, separation, irrigation, and aspiration of cataracts, residual cortical material and lens epithelial cells, vitreous aspiration and cutting associated with anterior vitrectomy, bipolar coagulation, and intraocular lens injection. The AutoSert® IOL Injector Handpiece is intended to deliver qualified AcrySof® intraocular lenses into the eye following cataract removal.

The AutoSert® IOL Injector Handpiece achieves the functionality of injection of intraocular lenses. The AutoSert® IOL Injector Handpiece is indicated for use with the AcrySof® lenses SN6OWF, SN6AD1, SN6AT3 through SN6AT9, as well as approved AcrySof® lenses that are specifically indicated for use with this inserter, as indicated in the approved labeling of those lenses.

WARNINGS: Appropriate use of Centurion® Vision System parameters and accessories is important for successful procedures. Use of low vacuum limits, low flow rates, low bottle heights, high power settings, extended power usage, power usage during occlusion conditions (beeping tones), failure to sufficiently aspirate viscoelastic prior to using power, excessively tight incisions, and combinations of the above actions may result in significant temperature increases at incision site and inside the eye, and lead to severe thermal eye tissue damage.

Good clinical practice dictates the testing for adequate irrigation and aspiration flow prior to entering the eye. Ensure that tubings are not occluded or pinched during any phase of operation.

The consumables used in conjunction with ALCON® instrument products constitute a complete surgical system. Use of consumables and handpieces other than those manufactured by Alcon may affect system performance and create potential hazards.

AEs/COMPLICATIONS: Inadvertent actuation of Prime or Tune while a handpiece is in the eye can create a hazardous condition that may result in patient injury. During any ultrasonic procedure, metal particles may result from inadvertent touching of the ultrasonic tip with a second instrument. Another potential source of metal particles resulting from any ultrasonic handpiece may be the result of ultrasonic energy causing micro abrasion of the ultrasonic tip.

ATTENTION: Refer to the Directions for Use and Operator’s Manual for a complete listing of indications, warnings, cautions and notes.