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Leading North American and European Glaucoma Leaders Highlight Significant Effectiveness and Favorable Safety Profile of ELIOS in Review Article

Ten independent clinical studies demonstrate significant intraocular pressure (IOP) lowering effect of ELIOS with few complications and no residual device remaining in the angle.

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Disclaimer

ELIOS Vision GmbH is the EU distributor of ELIOS manufactured by MLase AG, located at 82110 Germering, Industriestr. 17 and the FIDO laser applicator manufactured by WEINERT Fiber Optics GmbH, Mittlere-Motsch-Strasse 26, 96515 Sonneberg, Germany. ELIOS is CE marked and licensed for use in the EU in adult patients with glaucoma and is currently under investigational use in the US as part of an ongoing IDE study (FDA). Product feedback should be sent to productsurveillance@eliosvision.com.

The ExTra II (laser class 4) has the brand name ELIOS. The ExTra II is equivalent to ExTra and AIDA devices.

Caution: Investigational device – Limited by Federal (or United States) law to investigational use. ELIOS is not currently approved for use in the U.S.

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