EX-PRESS® Glaucoma Filtration Device

The EX-PRESS® Glaucoma Filtration Device was initially cleared by U.S. Food and Drug Administration (FDA) on March 26, 2002, and is a miniature stainless-steel glaucoma shunt developed as an alternative to trabeculectomy filtration surgery for patients with glaucoma.

The American Medical Association (AMA) assigned the EX-PRESS® Glaucoma Filtration Device procedure to CPT® 0192T effective July 1, 2008.

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

Coding Fact Sheet and Sample Claim Forms

For additional reimbursement support, contact us.

Additional Resources