FEMTO LDV Z8

FEMTO LDV Z8
Product Animation
The FEMTO LDV Z8 is compact and mobile and more than "just" another femtosecond laser. It is a highly advanced intraoperative multitool - capable of performing a wide variety of applications in corneal and lens surgery. Due to its innovative design, it can be integrated into your workflow efficiently.

FEMTO LDV Z8
Patient Education Z-Cataract                           

Laser assisted cataract surgery
(LACS) of a black cataract

by Dr. Izquierdo, Peru

Laser assisted cataract surgery (LACS) of a black cataract by Luis Izquierdo Jr., MD. The cataract pre-treatment was assisted by the Ziemer FEMTO LDV Z8. Visit www.femtoldv.com/z8 for further Information. The video is courtesy of Luis Izquierdo Jr., MD.

Cataract live surgery with the Ziemer FEMTO LDV Z8 femtosecond laser
by Prof. Szurman, Germany
Prof. Peter Szurman (Knappschaftsklinikum Suzlbach) was the first user of the low energy femtosecond laser, FEMTO LDV Z8, in Europe. In this video live surgery he performs femtosecond laser assisted phacoemulsification and showcases the use of this laser system as intraoperative tool. 

Laser assisted cataract surgery with the Ziemer FEMTO LDV Z8 
by Prof. Menapace, Austria
Prof. Rupert Menapace (AKH Wien) performs laser assisted cataract surgery (LACS) with the FEMTO LDV Z8.

 

Femtosecond laser-assisted cataract surgery with FEMTO LDV Z8 
by Prof. Prünte, Switzerland
Prof. Prünte is performing a femto cataract surgery with the FEMTO LDV Z8 from Ziemer Ophthalmic Systems AG.

FEMTO LDV Z8
Femto-Cataract Surgery
by Dr. Izquierdo, PhD, Peru
First experiences with the FEMTO LDV Z8 femto-cataract system.  

FEMTO LDV Z8
First experience at ESCRS 2013
by Jeffrey Machat, MD;
Minoru Tomita MD, PhD;   Jod Mehta, MD and David Allamby, MD

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.