Join us at AAO 2022 in Chicago on October 1-3

Join us at AAO 2022 in Chicago on October 1-3

Booth #4853
McCormick Place Convention Center
Booth #4853
McCormick Place Convention Center
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Visit us at our booth to learn about the OMNI® Surgical System and get hands-on demos

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Visit us at our booth to learn about the OMNI® Surgical System and get hands-on demos

OMNI is an elegant, implant free MIGS device that targets three points of resistance. It allows surgeons to customize a MIGS plan to lower IOP in adult patients with Primary Open Angle Glaucoma, either as a standalone glaucoma procedure or in combination with cataract surgery.
VISIT OMNI WEBSITE

Speaker Forum: The power of the OMNI Surgical System as a standalone intervention

Join us at AAO, booth #4853 and learn from 12 glaucoma experts on the power of the OMNI® Surgical System as a standalone MIGS intervention. This will be an excellent opportunity to learn from experienced users and talk peer-to-peer about cases, patient selection, ask questions, or learn tips and best practices.
Download Program
Join us at AAO, booth #4853 and learn from 12 glaucoma experts on the power of the OMNI® Surgical System as a standalone MIGS intervention. This will be an excellent opportunity to learn from experienced users and talk peer-to-peer about cases, patient selection, ask questions, or learn tips and best practices.
Standalone MIGS: Beyond Cataract Surgery
Leon Herndon, MD (moderator)
Deborah Ristvedt, DO
Arkadiy Yadgarov, MD

Saturday, October 1, 2022
11:00 AM - 11:45 AM
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Standalone Use of the OMNI Surgical System
Cathleen McCabe, MD (moderator)
Jason Bacharach, MD
Jai Parekh, MD

Saturday, October 1, 2022
1:30 PM - 2:15 PM
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Why Standalone MIGS with the OMNI Surgical System
Paul Singh, MD (moderator)
Analisa Arosemena, MD
Amir Cohen, MD

Sunday, October 2, 2022
10:00 AM - 10:45 AM
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Best practices in adopting Standalone MIGS
Nathan Radcliffe, MD (moderator)
Matthew Brink, MD
Zarmeena Vendal, MD

Sunday, October 2, 2022
1:30 PM - 2:15 PM
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OMNI Dry Labs at AAO

OMNI Dry Labs at AAO

Two dry labs will feature the OMNI Surgical System at AAO. Check the AAO program for more details.
Surgical Curriculum for Ophthalmology
Residents (SCOR) Common skills
transfer curriculum – Commonly used
MIGS Platforms and Anterior Segment
Repair Techniques
Grace Sun, MD; Shahzhad Mian, MD
Friday, 7:30 AM – 4:15 PM
MIGS: Devices and Incisional Techniques
Brian A Francis, MD; Steven Sarkisian MD
Session: LAB124A
Location: N230
Sunday, 8:00 AM - 10:00 AM

SION™ Surgical Instrument – The first bladeless goniotomy device

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SION™ Surgical Instrument – The first bladeless goniotomy device

AAO will be our first time providing demos of SION. With its signature bladeless design, SION is designed to facilitate a smooth, gentle goniotomy.
VISIT SION WEBSITE

Contact Us

For additional information, email us at glaucoma@sightsciences.com. Please visit OMNISurgical.com/ifu for the full instructions for use, warnings, precautions, and adverse event information. Visit SIONsurgical.com/ifu for the full instructions for use, warnings, precautions, and adverse event information. Booth events are not part of the official AAO program. The twelve presenters are paid consultants of Sight Sciences. To stay informed about future events, follow us on social media. 09/22 OM-2589-US-V1
Thank You

We appreciate your interest in Sight Sciences. A member of our team will review your inquiry and get back to you as soon as possible during business hours.

Thank you for submitting your registration confirmation for the Sight Power Club Incentive Trip.
A representative from Travelong of Summit will contact you directly to book your flight arrangement within the next 24 – 48 hours. Important information, including hotel, transportation, and activity confirmations and additional details regarding your registration, will be emailed to you separately by A2E Communications Group, leading up to the event. Should you have any questions pertaining to Sight Power Club, please contact Anna Saum, Meetings & Events Director, A2E Communications Group, at asaum@a2ecomms.com, or via phone at (973) 580-3557.
Disclamer

In providing these materials requested by you, the physician, Sight Sciences does not intend to support or endorse any presentations, communications, or other messages you may impart through the use of these materials.

If and when you use the materials in a presentation, communication, or other message, please include a disclaimer that the statements and opinions in the presentation/communication/message are entirely your own and are not supported or endorsed by Sight Sciences.

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Important Product Information for OMNI® Surgical System

OMNI® Surgical System IMPORTANT PRODUCT INFORMATION
Indications for Use

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.

Contraindications

Do 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.

Do 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.

Do not use the OMNI® Surgical System in quadrants with previous MIGS implants.

Please refer to the full Instructions for Use, available at omnisurgical.com, for warnings, precautions, and adverse event information.

Warnings

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

2. 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.

3. 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.

4. The surgeon should monitor the patient postoperatively for proper maintenance of intraocular pressure. If intraocular pressure is not adequately maintained after surgery, the surgeon should initiate appropriate management of intraocular pressure.

Potential adverse events

Adverse events that may be reasonably associated with the use of the OMNI® System in the eye include, but are not limited to, the following: anterior chamber shallowing, severe, prolonged, or persistent intraocular inflammation, endophthalmitis or other ocular infection, aqueous misdirection, Descemet’s membrane tear or detachment, intracorneal hematoma, choroidal effusion, suprachoroidal hemorrhage, corneal decompensation, corneal injury, corneal edema or opacification, unintended trabeculotomy, cyclodialysis cleft, hyphema, hypopyon, hypotony, hypotony maculopathy, IOL dislocation, cataract formation, iris injury, tear, or iridodialysis, loss of vitreous, perforation of sclera, posterior capsular bag rupture, proliferative vitreoretinopathy, pupillary block, pupillary membrane formation, retinal detachment, retinal dialysis, retinal flap tears, secondary surgical intervention, including, but not limited to, glaucoma surgery, and vitreous hemorrhage. Federal (USA) law restricts this device to sale, distribution, or use by or on the order of a physician.

Important Product Information

INDICATIONS FOR USE

The TearCare® System is intended for the application of localized heat therapy in adult patients with evaporative dry eye disease due to meibomian gland dysfunction (MGD), when used in conjunction with manual expression of the meibomian glands.

CONTRAINDICATIONS

    • The TearCare® System is contraindicated for patients with:
    • Recent (i.e. within the last 90 days) surgical procedure to the eye or eyelid.
    • Recent ocular injury.
    • History of Herpes Simplex or Herpes Zoster of the eye or eyelid.
    • Active ocular or periocular infection, inflammation or irritation.
    • Diminished or abnormal facial, periocular, ocular, or corneal sensation.
    • Ocular surface ulcers.
    • Hordeolum, stye, or chalazion.
    • Do not use the TearCare® System in patients under the age of 22 years.
    • Pacemakers or implantable cardiac defibrillators (ICD). Use of the TearCare® System may affect the performance of pacemakers or ICD’s due to electromagnetic interference (EMI). To avoid any potentially serious safety effects, patients with these implants should not be treated with the TearCare® System.
    • Known allergy to acrylate.
    • Known allergy to silicone tissue adhesives.
    • Known allergy to copper.

    WARNINGS

    • Do not use the TearCare® System outside the instructions for use. Doing so can result in unanticipated patient harm.
    • Do not attempt to connect the SmartHub™ or SmartLid™ directly to an electrical outlet of any kind.
    • Do not use the TearCare® System in or near an MRI suite or near a magnetic field. Serious injury can occur to a patient or technician if a TearCare® System is brought into an MRI suite.
    • The TearCare® System has not been tested in the presence of flammable anesthetics or other flammable agents in combination with air, nitrous oxide, or oxygen enriched environments.
    • Do not apply SmartLids to non-intact skin (i.e., skin with active abrasion, cut, burn, rash, inflammation, redness, etc.)

    PRECAUTIONS

    • Use of the TearCare® System in patients with eyelid abnormalities (e.g., entropion, ectropion, tumor, edema, blepharospasm, lagophthalmos, severe trichiasis, severe ptosis, etc.) may result in poor adhesion of the SmartLid™ to the eyelid and/or reduced benefit.
    • Use caution when using the TearCare® System in patients with ocular surface abnormalities (e.g. pterygium, pingueculum, corneal dystrophies, etc.) as the heat delivered by the System may aggravate these conditions.
    • Remove contact lenses from the patient’s eyes prior to use of the TearCare® System. Patients should wait 60 minutes after the completion of the TearCare® procedure before re-inserting contact lenses.
    • Do not apply the SmartLids™ to any other part of the patient’s body including the cornea. The SmartLids™ are only intended for application on the external surface of the patient’s eyelids.
    • It is important for patient to keep their eyes open (blinking is permitted) during treatment, to allow heat to dissipate off of the ocular surface.
    • Effectiveness of the TearCare®System has not been established in subjects for whom the treatment temperature is lowered from Warmth Level Setting #5 due to patient pain or discomfort.
    • Do not reuse the SmartLids™. Cross-contamination can occur if re-use is attempted.
    • Do not use a TearCare® System, its components, or accessories that appear damaged. Inspect all components for damage before each use.
    • The safety and effectiveness of the TearCare®System is not known in the following patient populations that were excluded in the OLYMPIA pivotal study: patients under 22 years of age, dry eye signs and symptoms other than meibomian gland dysfunction, severe signs and symptoms of dry eye due to meibomian gland dysfunction (OSDI > 79), mild signs and symptoms of dry eye due to meibomian gland dysfunction, and other study exclusions described in the TearCare®Instructions for Use.

    POTENTIAL ADVERSE EVENTS

    Potential adverse events associated with the use of the TearCare® System include the following:

    • Eyelid or eye pain requiring discontinuation of the treatment procedure
    • Eyelid irritation or inflammation*
    • Ocular surface irritation or inflammation*
    • Ocular symptoms (such as burning, redness, tearing, visual disturbance, redness)
    • Burn, erythema, or swelling of the eyelids
    • Conjunctival infection (moderate or severe)
    • Conjunctival abrasion
    • Corneal abrasion
    • Corneal deformation
    • Allergic or inflammatory reaction to medical adhesive on the SmartLid device
    • Formation of a chalazion or stye*
    • Decline in visual acuity*
    • Worsening of dry eye symptoms*
    • Increased discomfort or pain of ocular surface (grittiness, foreign body sensation, etc.)
    • Discomfort or pain of eyelids or orbit*
    • There is a potential risk of thermal injury to eye or eyelid based on the device design.
    Important Product Information for SION™ Surgical Instrument

    INDICATIONS FOR USE

    The SION™ Surgical Instrument is a sterile, single use, manually operated device used in ophthalmic surgical procedures to excise trabecular meshwork.

    CONTRAINDICATIONS

    Do not use the SION™ if there is inadequate corneal clarity, or poor visualization of angle structures or in any situations where the anterior chamber angle has been damaged (i.e., from trauma or surgery) or it may not be possible to pass the device through Schlemm’s canal.

    SION™ is contraindicated in patients: with angle recession, neovascular glaucoma, chronic angle closure, narrow angle glaucoma, narrow inlets with plateau iris, peripheral anterior synechiae, traumatic, malignant, or uveitic glaucoma; it is also contraindicated in patients who have had previous argon laser trabeculoplasty, ab interno devices implanted in or through Schlemm’s Canal, or prior incisional glaucoma surgery including trabeculotomy, goniotomy.

    WARNINGS

    Always maintain direct microscopic and gonioscopic visualization of the instrument tip during the procedure to avoid inadvertently damaging intraocular structures. Avoid touching the SION™ tip to any surfaces as this may damage it. Do not use the SION™ tip to create a corneal incision.

    POTENTIAL ADVERSE EVENTS

    Adverse events that may be reasonably associated with the use of the instrument include but are not limited to the following: anterior chamber shallowing, prolonged, or persistent intraocular inflammation, aqueous misdirection, choroidal effusion, suprachoroidal hemorrhage, Descemet’s membrane tear or detachment, corneal decompensation, corneal injury, corneal edema or opacification, intracorneal hematoma, cyclodialysis cleft, damage to posterior wall of Schlemm’s canal, hyphema, hypopyon, hypotony, hypotonic maculopathy, IOL dislocation, iris injury, tear, or iridodialysis, loss of vitreous, perforation of sclera, posterior capsular bag rupture, posterior capsule opacification, proliferative vitreoretinopathy, pupillary block, pupillary membrane formation, retinal detachment, retinal dialysis, retinal tears, vitreous hemorrhage, elevated IOP requiring treatment and endophthalmitis.