Health Canada Approved Indications: The Meridian Lapex-2000 LipoLaser is a non-invasive low-level laser therapy device indicated for use in body contouring and temporary reduction in the appearance of cellulite. The device utilizes cold read laser for deep tissue warming to enhance microcirculation for the reduction in the appearance of cellulite.
FDA Indications For Use: FDA 510(k)(k081962) The Lapex BCS is intended to emit energy in the visible and infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and/or the temporary relaxation of muscle.
The Lapex BCS LipoLaser is not approved for body contouring by the USFDA. Active physician use is currently an off-label application. In the US the regulations of the FDA permit physicians to use cleared/approved medical devices for other than intended indications. This practice is known as off-label use.
It is important to know 100% certainty of success cannot be assured as with any medical procedure. It is also important to note that in the vast majority of cases, supported by numerous clinical studies, patients achieve satisfactory results. Results may vary and therefore not meet expectations of all patients completing a full series of treatments.
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