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ELIOS Vision’s Excimer Laser Trabeculostomy Procedure Receives New CPT Codes from American Medical Association

Two Category III CPT codes are approved to report trabeculostomy ab interno by laser with or without the use of an ophthalmic endoscope. The trabeculostomy procedure restores the “natural flow” of aqueous fluid using the company’s non-thermal, precise excimer laser system, ELIOS ELT.

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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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