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Iridex gets US nod for new infrared laser:

Iridex has received US FDA 510(k) clearance for its solid-state Iris Medical IQ 810 infrared diode laser photocoagulator for treating retinal disorders and glaucoma. The system is designed to perform traditional and Minimum Intensity Photocoagulation (MIP) procedures in the office and operating room settings. According to the Mountain View, California firm, the product increases the clinical versatility for ophthalmologists through the use of its SmartWare interactive software feature with customisable settings, advanced waveform capability, and FiberCheck slit lamp adapter delivery device. FiberCheck allows doctors to quickly and easily verify the integrity of the fibre before treatment, which is increasingly important with the adoption of MIP procedures where endpoints are not visible, the company explained.

Iridex has received US FDA 510(k) clearance for its solid-state Iris Medical IQ 810 infrared diode laser photocoagulator for treating retinal disorders and glaucoma. The system is designed to perform traditional and Minimum Intensity Photocoagulation (MIP) procedures in the office and operating room settings. According to the Mountain View, California firm, the product increases the clinical versatility for ophthalmologists through the use of its SmartWare interactive software feature with customisable settings, advanced waveform capability, and FiberCheck slit lamp adapter delivery device. FiberCheck allows doctors to quickly and easily verify the integrity of the fibre before treatment, which is increasingly important with the adoption of MIP procedures where endpoints are not visible, the company explained.

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