Clareon Vivity Extended Vision Hydrophobic Intraocular Lens - FDA Registration CMDR-2025-04852

Access comprehensive regulatory information for Clareon Vivity Extended Vision Hydrophobic Intraocular Lens in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04852 and manufactured by Alcon Laboratories, Inc. - 6201 South Freeway, Fort Worth, Texas 76134-2099, USA Mfd. By: Alcon Research, LLC-246 Kyle Lane, Huntington, West Virginia, 25702 USA in United State. The device was registered on June 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Alcon Laboratories (Philippines), Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.