WaveLight FS200 Laser System - FDA Registration CMDR-2025-04640

Access comprehensive regulatory information for WaveLight FS200 Laser System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04640 and manufactured by Alcon Laboratories, Inc. - 6201 South Freeway, Fort Worth, Texas 76134-2099 USA Mfd. By: Wavelight GmbH - Am Wolfsmantel 5, 91058 Erlangen, Germany in USA. The device was registered on May 14, 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.