WaveLight INNOVEYES™ Sightmap Diagnostic Device - FDA Registration CMDR-2025-04467

Access comprehensive regulatory information for WaveLight INNOVEYES™ Sightmap Diagnostic Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04467 and manufactured by Alcon Laboratories, Inc.- 6201 South Freeway, Fort Worth, Texas 76134-2099, USA Mfd. By: WaveLight GmbH- Rheinstraße 8, 14513 Teltow, Germany in USA. The device was registered on May 07, 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.