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New World Medical Receives 510(k) Clearance for the VIA360™ Surgical System, Further Advancing Innovation in Ophthalmic Surgery

New World Medical, a leading innovator in ophthalmic surgical devices, is proud to announce that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its VIA360™ Surgical System, for the delivery of controlled amounts of viscoelas­tic fluid during ophthalmic surgeries.

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New World Medical Receives 510k Clearance for KDB GLIDE® Expanded Indication, Enhancing Glaucoma Treatment Options

New World Medical, a leading innovator in ophthalmic surgical devices, is proud to announce the receipt of 510(k) indication expansion from the U.S. Food and Drug Administration (FDA) for KDB (Kahook Dual Blade) GLIDE to be used for the reduction of IOP in adult patients with primary open-angle glaucoma (POAG) during cataract surgery or as a standalone procedure.

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