FEMTOSECOND WORKSTATION

TECHNOLAS^®Femtosecond Workstation

Versatile advanced technology

The TECHNOLAS 520F is a highly flexible tool used for treating a broad variety of indications. The 520F procedures are personalized via the easy to use CUSTOMFLAP^™ and CUSTOMSHAPE^® software, which provide unrivaled control. The 520F used combination with the Curved Patient Interface approach makes all the difference:

No flattening of the cornea
Improved patient comfort, reduced increase of IOP
Truly curved cuts, full control
Patient interface suction is permanently computer controlled

Latest Innovations

A number of new features have been incorporated into the 520F system, providing users with a enhanced ease-of-use, advanced options and a improved surgical workflow.

A new laser head - A new laser head is now installed in the system to improve accuracy of outcomes providing excellent stromal bed quality
Faster flap procedures - the laser now operates at 80kHz to allow flaps to be produced in only 20 seconds
New centration software - Allows surgeons to recentre the procedure under the curved interface via the software

Features

Refractive:

INTRACOR^®*
Minimally invasive technique for the correction of presbyopia – available since 2009*

Lasik flaps:

80 kHz CUSTOMFLAP^™
Using the TECHNOLAS 520F for a CUSTOMFLAP is easy, predictable, and customizable.

shorter treatment times
variable diameter
smoother stromal bed
selectable flap thickness
free choice of hinge position

Therapeutic*:

Penetrating and Lamellar Keratoplasty (PKP/LKP)
Femtosecond Laser assisted Endothelial Keratoplasty (FLEK)
Tunnels for Intrastromal Ring Segments (ICRS)
Arcuate cuts for Astigmatic Keratotomy (AK)

* INTRACOR and CUSTOMSHAPE are CE marked but NOT approved for use in the US. INTRACOR, CUSTOMSHAPE and CUSTOMFLAP are not approved in all countries.

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

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