ZEISS Announces U.S. FDA Clearance of the QUATERA 700, a Revolution in Phaco Technology
JENA, Germany and DUBLIN, Ireland , April 20, 2022 /PRNewswire/ -- Today, ZEISS Medical Technology announced the U.S. Food and Drug Administration (FDA) has cleared the QUATERA® 700*, a revolution in phaco technology. It includes the ZEISS patented QUATTRO Pump® which delivers an exceptional level of chamber stability independent of intra-ocular pressure (IOP) and flow.
- JENA, Germany and DUBLIN, Ireland, April 20, 2022 /PRNewswire/ -- Today, ZEISS Medical Technology announced the U.S. Food and Drug Administration (FDA) has cleared the QUATERA 700 *, a revolution in phaco technology.
- It includes the ZEISS patented QUATTRO Pump which delivers an exceptional level of chamber stability independent of intra-ocular pressure (IOP) and flow.
- The ZEISS QUATERA 700 is designed to increase a surgeon's workflow efficiency from the clinic to the operating room (OR), enabling one digitally integrated surgical workflow.
- 59 percent are held by Carl Zeiss AG, one of the world's leading groups in the optical and optoelectronic industries.