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Business of Optometry News
FDA fast tracks urcosimod for neuropathic corneal pain
The FDA granted fast track designation to urcosimod to treat neuropathic corneal pain, according to a press release from Okyo Pharma.
JP Morgan banker says innovation will drive ophthalmology through current market cycle
LOS ANGELES — Today’s volatile environment is impacting the markets, but innovation in ophthalmology will drive the sector and lead to increased value, a JP Morgan managing director told attendees at SightLine.
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VIDEO: Bausch + Lomb provides update on return to market of enVista IOLs
LOS ANGELES — In this Healio Video Perspective from the ASCRS meeting, Anthony Wallace, of Bausch + Lomb, provides further details on the return to market of enVista IOLs.
VIDEO: Nordic, Harrow launch generic Maxitrol
LOS ANGELES — Nordic Pharma and Harrow partnered to launch an authorized generic of Maxitrol, Nordic President Philip Gioia said in this Healio Video Perspective from SightLine.
Tired of pleasing ‘corporate masters,’ physician union membership rises
Union membership among health care professionals in the United States, including physicians, is on the rise, which could have seismic implications in work patterns and patient care in an increasingly corporatized medical system.
Optical products from China now tariffed as high as 178%
The recent increase in tariffs on Chinese imports has resulted in tariffs as high as 178% on some optical products, which could significantly affect the cost of eyeglasses and other products, according to a Vision Council press release.
FDA clears Luminopia for amblyopia in children aged 8 to 12 years old
The FDA cleared Luminopia, a virtual reality-based therapeutic for amblyopia, for use in children aged 8 to 12 years old, adding to its existing approval in children aged 4 to 7 years old, according to a press release.
10 common mistakes made in health savings accounts: What physicians need to know
Health savings accounts are a powerful tool for managing health care expenses, offering significant tax advantages and flexibility.
FDA does not approve additional extended dosing intervals for Eylea HD
The FDA issued a complete response letter for a supplemental biologics license application, in which it did not approve extending the dosing intervals for Eylea HD, according to a press release from Regeneron.
FDA clears Leos laser system for glaucoma
The FDA granted 510(k) clearance for Leos, a laser endoscopy ophthalmic system for a more intuitive laser endoscopic cyclophotocoagulation procedure, according to a press release from BVI Medical.
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Headline News
Closed CDC lab was cornerstone of national, global STI science
June 04, 20257 min read -
Headline News
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June 06, 20256 min read -
Headline News
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