Ophthalmic Devices

IRIDEX Issues Voluntary Recall of TruFocus LIO Premiere™ Laser Indirect Ophthalmoscope

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IRIDEX Issues Voluntary Recall of TruFocus LIO Premiere™ Laser Indirect Ophthalmoscope

Register to receive a free U.S. Market Report Suite for Interventional Ophthalmic Devices – MedSuite report synopsis and brochure IRIDEX Corporation (“Company”) initiated a voluntary recall of a specific laser accessory called the TruFocus LIO Premiere™.  The LIO is a headmounted indirect ophthalmoscope that connects to an IRIDEX laser console and is used to view and perform

iData ResearchIRIDEX Issues Voluntary Recall of TruFocus LIO Premiere™ Laser Indirect Ophthalmoscope
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Optovue First in US to Receive FDA Clearance for Corneal Epithelial Thickness Mapping

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Optovue First in US to Receive FDA Clearance for Corneal Epithelial Thickness Mapping

Epi-mapping is the first non-contact, quantitative method for corneal epithelia and stromal measurements, and it is the first and only FDA-cleared product indicated to provide corneal epithelia and stromal measurements that aid in the diagnosis, documentation and management of ocular health and diseases in the adult population.

iData ResearchOptovue First in US to Receive FDA Clearance for Corneal Epithelial Thickness Mapping
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