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EX-PRESS® GLAUCOMA FILTRATION

The EX-PRESS® Glaucoma Filtration Device was initially cleared by U.S. Food and Drug Administration on March 26, 2002.

The guidance documents and sample forms below are provided to assist you in the coding, billing, and reimbursement process.

Guidance Documents

Additional Resources

An explanatory video for surgeons and staff that suggests how to talk to patients about ATIOL charges using an easy-to-understand, two-service billing concept.