Home » Glaukos’ iPrime Viscodelivery System Gets FDA’s 510(k) Clearance
Glaukos’ iPrime Viscodelivery System Gets FDA’s 510(k) Clearance
San Clemente, Calif.-based Glaukos has received the FDA’s 510(k) clearance for its iPrime viscodelivery system for use in ophthalmic surgery.
iPrime is a sterile, single-use, minimally invasive product designed to deliver viscoelastic fluid during eye surgeries.
A pioneer in minimally invasive glaucoma surgery, Glaukos specializes in novel therapies to treat glaucoma, corneal disorders and retinal diseases.
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