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The surgeon should monitor the patient postoperatively for proper maintenance of intraocular pressure. Maintain direct microscopic or gonioscopic visualization of the cannula tip and microcatheter tip at all times during the procedure to facilitate advancement and to avoid inadvertently damaging intraocular structures, kinking the microcatheter or unintended tearing of trabecular meshwork.Ĥ. Perform gonioscopy prior to taking a patient to surgery to exclude congenital anomalies of the iridocorneal angle, anterior segment dysgeneses, peripheral anterior synechiae (PAS), rubeosis, and any other angle abnormalities that could lead to improper placement of the cannula and microcatheter and pose a hazard.ģ. The following conditions may prohibit sufficient visualization required for safe and successful cannula and microcatheter placement: corneal edema, corneal haze, corneal opacity, or any other conditions that may inhibit gonioscopic view of the iridocorneal angle and intended cannula entry location.Ģ.

Do not use in cases where there is insufficient visibility to properly see the iridocorneal angle.

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Please refer to the full Instructions for Use, available at, for warnings, precautions, and adverse event information. Contraindicationsĭo not use the OMNI ® in any situations where the iridocorneal angle is compromised or has been damaged (e.g., from trauma or surgery), since it may not be possible to visualize the angle or to properly pass the microcatheter.ĭo not use the OMNI ® in patients with angle recession neovascular glaucoma chronic angle closure narrow-angle glaucoma traumatic or malignant glaucoma or narrow inlet canals with plateau iris.ĭo not use the OMNI ® Surgical System in quadrants with previous MIGS implants. The OMNI ® Surgical System is indicated for canaloplasty (microcatheterization and transluminal viscodilation of Schlemm’s canal) followed by trabeculotomy (cutting of trabecular meshwork) to reduce intraocular pressure in adult patients with primary open-angle glaucoma. OMNI ® Surgical System IMPORTANT PRODUCT INFORMATION Indications for Use