Clear Corneal Incisions & Arcuate Incisions

  • Custom-designed incisions
  • Topographically matched
  • Added precision and reproducibility
  • Intrastromal incisions possible

Arcuate Incisions (ARC)

Arcuate Incisions (ARC)

Added precision and reproducibility

Operating with very low pulse energy and very short pulse width, but with very high pulse frequencies, the FEMTO LDV assures a very high precision and reproducibility in comparison to manual technique.

Advantages at a glance

  • Complete control of position and angle
  • Higher precision in dimension and depth
  • Automated construction for higher reproducibility
  • Clinical outcome more predictable and constant

Specifications - ARC

  • Up to three arc-shaped incisions
  • Penetrating and intrastromal (partial thickness) incisions
  • Up to 10 mm diameter
  • Precise positioning and adjustment

Clear Corneal Incisions (CCI)

Clear Corneal Incisions (CCI)

Topographically matched incisions

Individual incision construction - uni, bi or triplanar - are available with this highly flexible software. Due to the custom-designed and more angled architecture, enhanced treatments can be supported.

Advantages at a glance

  • Self-sealing incisions (no sutures needed)
  • Help preventing post-op endophthalmitis
  • Reproducible dimensions
  • Tailored and flexible geometry

Specifications - CCI

  • One main and up to two side port incisions
  • Single and multi-plane geometries (1,2 or 3 segments)
  • Programmable tissue bridge possible
  • Up to 10 mm diameter
  • Individual positioning

Availability
The FEMTO LDV Z2, Z4, Z6 and Z8 are CE marked and FDA cleared. For some countries, availability may be restricted due to regulatory requirements; please contact Ziemer for details. Presbyopia treatments occur exclusively by a pocket creation and the implantation of a corresponding corneal inlay of a third party. Availability of related corneal inlays and implants may vary according to policy of the individual manufacturers and regulatory status in the individual countries. To comply with FDA regulations, devices for sale in the U. S. do not mention 'Presbyopia' on the panels.