Alcon reported on Friday the availability of the pre-loaded CyPass Ultra System for use in adult patients with mild-to-moderate primary open-angle glaucoma undergoing cataract surgery.
This new pre-loaded CyPass Ultra system is expected to be available to surgeons in May 2018. The new system reduces the number of steps required to implant the CyPass Micro-Stent, a microinvasive glaucoma surgery (MIGS) device, to help deliver safe, consistent, long-term intraocular pressure (IOP) control, added the company.
The company said the CyPass Ultra System includes a pre-loaded CyPass Micro-Stent, which is housed in a loader tip attached to a hand-held surgical instrument called the CyPass applier. The CyPass Micro-Stent is a prescription medical device that is indicated for use in conjunction with cataract surgery for the reduction of IOP in adult patients with mild-to-moderate primary open-angle glaucoma.
Under the company's randomized, multicenter clinical trial comparing cataract surgery with the CyPass Micro-Stent to cataract surgery alone, the study findings show long-term reduction in intraocular pressure and minimal effects on refractive outcomes versus cataract surgery alone.
In conjunction, the company's CyPass Ultra System, along with the data from the clinical value of the CyPass Micro-Stent, will be presented at the American Society of Cataract and Refractive Surgery (ASCRS) annual meeting this year.
Alcon is engaged in eye care and a division of Novartis, a healthcare solutions company headquartered in Basel, Switzerland.
OSR Holdings to acquire Korean non-invasive glucose monitor developer Woori IO
Autonomix Medical secures new US patent to expand precision nerve-targeted therapies
MedHub-AI's AutocathFFR receives national reimbursement approval in Japan
Microbot Medical secures first Japanese patent for Liberty robotic system following FDA clearance
Polarean Imaging signs new supply agreementwith UVA Health for clinical Xenon MRI
Femasys partners with Kebomed to expand FemBloc permanent birth control in France and Benelux
Implantica receives positive FDA feedback on final RefluxStop PMA submission
Tempus secures FDA clearance for RNA-based xR IVD diagnostic device
Shoulder Innovations expands I-Series portfolio with launch of InSet 70 Humeral Stem
GSK commits USD30bn to US R&D and manufacturing expansion
ArtPlayer Promotes Elderly Wellbeing with Digital Signage and Streaming Art in Finnish Care Homes
Implantica produces 10,000 RefluxStop units ahead of planned US launch
Elute partners Spartan Medical
Saol Therapeutics receives US FDA Complete Response Letter for SL1009 (DCA) in PDCD