Andrew Technologies, LLC has received FDA 510 (k) clearance for Autologous Fat Transfer, so that the adipose tissue (fat) harvested during a HydraSolve liposuction procedure can be reinjected into the same patient for rejuvenation or augmentation. No other liposuction device has been FDA cleared for this use.
HydraSolve™ is a novel liposuction device based on the same patented Tissue Liquefaction Technology™ that was launched in 2003 by Alcon as the AquaLase® Liquefaction Device, a modality on the Infiniti Vision System, for precision cataract surgery.
Hydrasolve™ combines natural saline solution with low levels of pressure and temperature, to liquefy only targeted fat tissue. Because fat tissue is liquefied, the cutting of fat by forceful thrusts of the cannula is no longer required.
The specially designed HydraSolve™ cannula is also manufactured with aperture edges that have a rounded radius of curvature that do not cut tissue. It is the energised saline stream, inside the cannula, that liquefies targeted fat tissue while preserving blood vessels, nerves and connective tissue integrity. HydraSolve™ achieves liquefaction of fat tissue by cell disaggregation, not by emulsification and the lysing of cell membranes.
Dr Mark S. Andrew, Chief Scientific Officer of Andrew Technologies stated, ‘We are extremely pleased to take a leading role in providing technology for autologous fat grafting that we believe can improve the process for the surgeon and the outcome for the patient.’
Tom Albright, CEO of Andrew Technologies says: ‘We are thrilled to achieve our second FDA clearance in less than 6 months — as a start-up medical device company that is quite an accomplishment. Also, since autologous fat grafting is a major focus for aesthetic medicine, we are pleased to offer our surgeons the first liposuction device that is FDA cleared for the harvesting of adipose (fat) tissue for transfer.’