Ex-Press™ Glaucoma Filtration Device - FDA Registration CMDR-2024-03200

Access comprehensive regulatory information for Ex-Press™ Glaucoma Filtration Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03200 and manufactured by Alcon Laboratories, Inc.- 6201 South Freeway, Fort Worth, Texas 76134-2099, USA Mfd. By: Alcon Research LLC- 714 Columbia Avenue, Sinking Spring, Pennsylvania 19608, USA in USA. The device was registered on August 29, 2024.

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.