JENA, GERMANY and DUBLIN, CA--(Marketwired - Sep 15, 2016) - The Medical Technology Business Group of ZEISS announces the introduction in the US of the VisuMax ® Small Incision Lenticule Extraction ...

Christenbury Eye Center in Charlotte, N.C., has announced it has invested in a Zeiss VisuMax femtosecond laser, according to a news release. The VisuMax laser is used to create the corneal flap, the ...

The US Food and Drug Administration (FDA) today approved the VisuMax Femtosecond Laser (Carl Zeiss Meditec) to remove a sliver of corneal tissue to reduce or eliminate myopia in certain adults aged 22 ...

Please provide your email address to receive an email when new articles are posted on . The VisuMax femtosecond laser and the Moria M2 automated microkeratome yielded similar safety and efficacy ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. The FDA approved the VisuMax 800 with SMILE pro software ...

DUBLIN, Calif. & JENA, Germany--(BUSINESS WIRE)--Carl Zeiss Meditec announced its intention to initiate a US clinical trial of the ReLEx smile procedure for the correction of myopia, having received ...

The U.S. Food and Drug Administration today approved the VisuMax Femtosecond Laser for the small incision lenticule extraction (SMILE) procedure to reduce or eliminate nearsightedness in certain ...

To evaluate the safety and efficacy of implanted Kerarings in patients with mild, moderate, and severe keratoconus. Keratoconus is the most common form of corneal ectasia in which progressive corneal ...

"With the growing interest in laser vision correction in China, the market needs innovative technology that enhances surgical outcomes, safety and efficiency to benefit both surgeons and their ...

The U S Food and Drug Administration approved the VisuMax Femtosecond Laser manufactured by Carl Zeiss Meditec Inc., of Dublin in California for the small incision lenticule extraction (SMILE) ...