Teneo excimer laser platform approved for LASIK correction of myopia, myopic astigmatism
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Key takeaways:
- The Teneo excimer laser platform is indicated for the correction of myopia and myopic astigmatism.
- The platform offers advances in accuracy, efficiency and usability.
The FDA approved the Teneo excimer laser platform for LASIK vision correction surgery for myopia and myopic astigmatism, according to a press release from Bausch + Lomb.
The platform includes a high-speed laser that operates at 500 Hz and an advanced eye tracker that operates at 1,740 Hz.
Teneo is the smallest excimer laser unit available in the U.S. and is designed to streamline the surgical process with a customizable graphical user interface touchscreen. The software treats the manifest refraction and eliminates the need for a nomogram, and the platform has a 360° swiveling microscope that adapts to surgeon height and posture.
It is indicated for LASIK to reduce or eliminate myopic astigmatism up to –10 D manifest refraction spherical equivalent, with sphere between –1 D and cylinder between 0 D and –3 D, in patients who are 22 years of age or older with a stable refraction for 12 months.
The approval is the first in nearly 2 decades for an excimer platform, according to the release.
“FDA approval of Teneo represents a major milestone for the advancement of laser vision correction technology in the United States,” George O. Waring IV, MD, FACS, founder and medical director of Waring Vision Institute, Mt. Pleasant, South Carolina, said in the release. “In addition to the technological advantages Teneo offers, the open air feeling around the laser and quiet performance contribute to a comfortable experience for the patient.”