Clinical Applications

This page provides a summary of the iTrack™ Advance clinical applications by region. Indications and available device functions vary depending on where the device is used. For complete information, including contraindications, warnings, precautions and adverse events, please refer to the Instructions for Use (IFU).

The iTrack™ Advance has a US Food and Drug Administration (FDA) 510(k) #K221872 for the treatment of open-angle glaucoma.

Indications for use

The Nova Eye iTrack™ Advance is indicated for fluid infusion or aspiration during surgery. The Nova Eye iTrack™ Advance is indicated for the cutting or disruption of the trabecular meshwork during goniotomy procedures.* The Nova Eye iTrack™ Advance is indicated for catheterization and viscodilation of Schlemm’s canal to reduce intraocular pressure in adult patients with open-angle glaucoma.

* The iTrack™ Advance cutting function (goniotomy) is a Class 1 510(k) exempt device function that is not specifically indicated for the reduction of intraocular pressure (IOP) or the treatment of open-angle glaucoma.

The ab interno surgical technique is not an on label indication for the iTrack™ Advance in the USA.

About Canaloplasty

Canaloplasty is a microcatheter-based glaucoma procedure that uses 360° catheterization of Schlemm’s canal followed by viscodilation with viscoelastic. The goal is to support aqueous outflow through the conventional pathway by addressing resistance along the trabecular meshwork, Schlemm’s canal and collector channels.

About Goniotomy

Goniotomy is an angle-based procedure that cuts or disrupts the trabecular meshwork to enhance access to the conventional outflow pathway. This approach is designed to improve trabecular outflow by creating a direct opening through the trabecular meshwork.

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Not all products are available in all regions or countries. Please contact your Nova Eye representative for more information.
Surgeons in the Operating room using itrack devices
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*In-house bench testing data using a proprietary optical rheology test apparatus to assess the change in viscosity over time during viscoelastic delivery with the iTrack™ Advance. Bench testing data may not be indicative of clinical outcomes. Clinical effects depend on anatomy and surgical technique. Results may vary.

Disclaimer

North America

The iTrack™ Advance has a CE Mark (Conformité Européenne) 2862 and US Food and Drug Administration (FDA) 510(k) #K221872 for the treatment of open-angle glaucoma.

INDICATIONS (USA): The iTrack™ Advance is indicated for fluid infusion or aspiration during surgery. The Nova Eye iTrack™ Advance is indicated for the cutting or disruption of the trabecular meshwork during goniotomy procedures.* The Nova Eye iTrack™ Advance is indicated for catheterization and viscodilation of Schlemm’s canal to reduce intraocular pressure in adult patients with open-angle glaucoma.The ab interno surgical technique is not a cleared indication of the iTrack™ Advance in the USA.

*The iTrack™ Advance cutting function (goniotomy) is a Class 1 510(k) exempt device function that is not specifically indicated for the reduction of intraocular pressure (IOP) or the treatment of open-angle glaucoma.

CONTRAINDICATIONS (USA): The iTrack™ Advance is not intended to be used for catheterization and viscodilation of Schlemm’s canal to reduce intraocular pressure in eyes of patients with the following conditions: Neovascular glaucoma; Angle-closure glaucoma; Previous surgery with resultant scarring of Schlemm’s canal.

PRECAUTIONS (USA): The iTrack™ Advance should be used only by physicians trained in ophthalmic surgery. Knowledge of surgical techniques, proper use of the surgical instruments, and post-operative patient management are considerations essential to a successful outcome.

© 2026. Nova Eye, Inc. E&OE. Patents pending and/or granted. iTrack™ Advance, iTrack™, ViscoInjector™ and iLumin™ are trademarks of Nova Eye, Inc.