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"The precision and predictability of femtosecond laser technology, when applied to critical steps in refractive cataract surgery; such as CCIs, LRIs, capsulorhexis and lens fragmentation, will allow more cataract surgeons to feel comfortable using these procedures to optimize visual outcomes. This will be especially true, when inserting some of the newer toric, multifocal and accommodating high performance intraocular lenses".

—R. L. Lindstrom, MD
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The LensAR Laser System™ integrates proprietary automated biometry, advanced ocular imaging and measurement technology, 3D-CSI™ (Confocal Structured Illumination) with an advanced ultra short pulse laser. The system is designed to bring a level of precision to the refractive cataract procedure never before thought possible by automating most of the manual incisions and allow for the reduction of ultrasound power required substantially, in all grades of cataracts. The system will perform the CCl's. LRI's. Capsulotomies and Lens Fragmentation automatically after taking a 3D image and accurately measure all of the ocular structures from the front surface of the cornea to the posterior surface of the lens.

AAO 2009 Surgeon Presentations
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Patient Docking 3D CSI
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Capsulotomy Fragmentation
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LRI's and CCI's Presbyopia
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Overview The Impact of Tilt
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The LensAR Laser System Effective Lens Position
   
 

 

AAO 2009 Surgeon Presentations
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Laser Capsulotomies: Size and Shape

Laser Capsulotomies: Strength Study

Crystalline Lens Softening for Presbyopia

 
 

 

“It is important to note that the LensAR Laser System was initially conceived and designed to correct presbyopia; and early clinical data established that it not only softened the lens, it showed the potential to restore its natural flexibility and accommodative power. By applying this level of precision and accuracy to cataract surgery the potential to increase predictability of outcomes is significant."

—Ronald R. Krueger, MD, MSE
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The LensAR Laser System is cleared by the FDA for anterior capsulotomy and laser phaco fragmentation.
For other indications it is an investigational device limited by United States law to investigational use only.