Learn all about the VICTUS® Femtosecond Laser Platform

Learn more about the new TECHNOLAS® TENEO™ 317 Excimer Laser




Upcoming Events

NOG – Nederlands Oogheelkundig Gezelschap
26th – 29th March 2014
Maastricht, Netherlands
www.congresdienst.nl


WOC/APAO - World Ophthalmology Congress/Asia Pacific Academy of Ophthalmology
2nd – 6th April, 2014
Tokyo, Japan
www.woc2014.org

ASCRS - American Society of Cataract & Refractive Surgery
25th – 29th April, 2014
Boston, USA
www.ascrs.org



What is New











 
Some of the products and/or specific features as well as the procedures featured on this website may not be approved in your country and thus may not be available there. The VICTUS platform has CE Marking for capsulotomy, lens fragmentation, arcuate corneal incisions, corneal incisions, LASIK flap, INTRACOR®, penetrating keratoplasty and intrastromal channel incisions for intracorneal ring segments. Indications may vary by country. The VICTUS platform is cleared in the United States for creation of a corneal flap in patients undergoing LASIK surgery or other treatment requiring initial lamellar resection of the cornea, anterior capsulotomy during cataract surgery, and arcuate incisions during cataract surgery. The TECHNOLAS TENEO 317 is CE marked but NOT approved for use in the US. The TECHNOLAS TENEO 317 is not approved in all countries.

SUPRACOR excimer laser treatment and INTRACOR are CE marked but NOT approved for use in the US. SUPRACOR excimer laser treatment and INTRACOR and are not approved in all countries. Please contact our regional representative regarding individual availability in your respective market.

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