Wednesday, August 5, 2026
FDA Clears Omni Ultra for POAG
Sight Sciences's next-generation MIGS device is indicated for canaloplasty and trabeculotomy in adults with primary open-angle glaucoma.
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Ophthalmology Management
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Retinal Physician
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Glaucoma Physician
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Ophthalmic Professional
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The Ophthalmic ASC
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Presbyopia Physician
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Corneal Physician
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New Retinal Physician
Wednesday, August 5, 2026
Sight Sciences's next-generation MIGS device is indicated for canaloplasty and trabeculotomy in adults with primary open-angle glaucoma.
Wednesday, July 29, 2026
The proposed acquisition of Lumibird Medical would include established SLT and Nd:YAG laser systems used in glaucoma care.
Monday, July 27, 2026
The study will evaluate the Preserflo MicroShunt in adult patients with primary open-angle glaucoma who failed previous medical and surgical treatment.
Friday, July 24, 2026
The application to the FDA is supported by data from the phase 3 Mont Blanc and Denali trials in open-angle glaucoma and ocular hypertension.
Wednesday, July 22, 2026
The statement was prompted by insurers' inconsistent coding and reimbursement policies for ab interno cyclodialysis procedures, which have led to confusion and claim denials in some cases.
Friday, July 17, 2026
The proposed Medicare Physician Fee Schedule for 2027 includes changes to same-day E/M payment, practice expenses, and physician reimbursement.
By Jim Gallagher, senior managing editor
Monday, July 13, 2026
The study did not achieve its primary endpoint of replicating visual function improvements observed in a smaller phase 1/2a study following 28 days of topical administration for glaucoma.
Monday, July 13, 2026
The Bausch + Lomb study did not meet its primary endpoint, defined as change from baseline in visual field mean deviation at day 28 (exit, hour 2).
Friday, July 10, 2026
Prednisolone acetate ophthalmic suspension, USP, 1%, manufactured by Lupin Limited, has been recalled due to the presence of a foreign substance.
Thursday, June 25, 2026
Glaukos is evaluating its iLution platform in patients with Demodex blepharitis.
Tuesday, June 23, 2026
The acquisition of Perfuse Therapeutics adds an investigational phase 2 implant to Bayer's ophthalmology portfolio.
Tuesday, June 23, 2026
The collaboration aims to advance visual function assessment through virtual reality technology and software-driven innovation.
Wednesday, June 17, 2026
Zolymbus (bimatoprost ophthalmic gel) 0.01% is indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension
Monday, May 18, 2026
SpyGlass Pharma’s drug-eluting IOL implant receives a Category III code; phase 3 trials continue enrollment.
Tuesday, May 12, 2026
The connected system enables remote monitoring of overnight patient adherence.
Wednesday, May 6, 2026
The sustained-release intraocular implant program focuses on visual field preservation and ischemia-related damage.
Tuesday, March 31, 2026
The Interventional Glaucoma Network will integrate clinical data to accelerate research, enrollment, and outcomes tracking.
Tuesday, March 31, 2026
The system is designed to provide durable canal support without permanent synthetic implants.
Thursday, March 26, 2026
Smaller drops were associated with improved pressure control and fewer adverse effects.
Monday, March 23, 2026
Data from the pivotal US study shows significant IOP reduction and consistent safety for the excimer laser procedure.
Friday, March 13, 2026
New online tool aims to improve patient understanding of eyedrop use and adherence.
Thursday, March 12, 2026
Johnson & Johnson’s EDOF lens aims to expand visual range while maintaining contrast sensitivity.
Wednesday, March 11, 2026
The new brand reflects the company’s expansion beyond visual field testing to a broader diagnostic platform with integrated clinical workflows.
Tuesday, March 10, 2026
Data from the phase 1/2 trial demonstrate sustained IOP reduction and preserved visual acuity in OAG and OHT patients.
Tuesday, February 10, 2026
BVI announces the first US implantations of the presbyopia-correcting trifocal IOL following FDA clearance last fall.
Tuesday, February 3, 2026
NMPA clearance expands access to advanced ophthalmic visualization platforms.
Wednesday, January 28, 2026
Updated labeling permits re-administration of the intracameral travoprost implant under a defined treatment protocol.
Monday, January 26, 2026
The first patient has been enrolled in the ADAPT trial, which will assess the safety and effectiveness of a titratable shunt for IOP control.
Friday, January 23, 2026
A pair of registrational trials will compare the company’s bimatoprost-eluting lens to a standard lens plus drops.
Tuesday, January 13, 2026
The platform is designed to support continuous glaucoma surveillance using home-based testing and remote care management.
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