Iridex transilluminated probe for glaucoma treatment receives CE Mark approval

March 20, 2018
The probe is powered by the company's Cyclo G6 glaucoma laser system.

Iridex (Mountain View, CA) has received CE Mark regulatory approval in Europe for its G-Probe Illuminate probe, which combines transillumination and a laser fiber for targeted transscleral cyclophotocoagulation (CPC; a glaucoma treatment). The probe, which received FDA clearance and was launched in early 2017, is powered by the company's Cyclo G6 glaucoma laser system. The system features built-in transillumination to optimize placement of the probe and therapeutic outcomes.

Related: Iridex ophthalmic laser system for glaucoma treatment receives CE Mark approval

Studies have shown the ciliary body, the target tissue for a CPC treatment, naturally varies in location between patients, and cases of abnormal ocular size, high myopia, and post-corneal transplants generate even more challenges. The G-Probe Illuminate may improve the ability of physicians to locate the ciliary body and deliver the laser treatment in a more targeted manner.

The G-Probe Illuminate may be used in the operating room or as an outpatient, office-based procedure for treating glaucoma.

For more information, please visit www.iridex.com.

About the Author

BioOptics World Editors

We edited the content of this article, which was contributed by outside sources, to fit our style and substance requirements. (Editor’s Note: BioOptics World has folded as a brand and is now part of Laser Focus World, effective in 2022.)

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