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Lutronic® Announces FDA Clearance for INFINI™, an Ideal Solution for Wrinkle Reduction Through 3-D Volumization
Date:7/23/2013

Fremont, California (PRWEB) July 23, 2013

Lutronic, a global leader of lasers and therapeutic devices for aesthetic and medical applications, announced today that the INFINI™ is now available for sale in the USA, following its receipt of the 510(k) clearance from the United States Food and Drug Administration (FDA). "The INFINI is a device that provides a new dimension in RF technology that will be well received by USA physicians and patients alike,” stated Ann Marie Collier, Global Products & Marketing Officer. “Previously released outside of the USA, the Infini is clinically proven in Europe, Asia, the Middle East and South America and has enabled Investigators and Customers to perform thousands of procedures. Their collective input indicates Infini has many technologically advanced features physicians appreciate and clinical outcomes their patients love, for a positive impact on clinic business.”

Infini’s approach is an ideal solution to create targeted coagulation zones in aging, sagging skin with wrinkles. Complete control over treatment depth and energy levels enables a multi-layered treatment approach with no electrothermal damage to the epidermis.

“Infini’s proven design delivers improved wrinkle reduction through 3-dimensional energy delivery to volumize tissue and deliver improved outcomes for a broad range of skin types, including darker skin types and tanned skin,” said R. Glen Calderhead, PhD and Vice President of Scientific Affairs at Lutronic. “Infini can deliver the RF energy into the dermis up to 3.5 mm deep, which has many clinical benefits. Adjustable target depth control allows for precise and controllable fractionated coagulation zones within a specific layer of the dermis; physicians can choose to provide mild to aggressive treatments, even in delicate areas. Additionally, the treatment is well tolerated by patients, thanks to the ComfortFlow™ technology.”

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