The lpg cellu m6 keymodule gets fda clearance for treating lymphedema - free-press-release.com
The LPG Cellu M6 Keymodule Gets FDA Clearance for Treating Lymphedema - Free-Press-Release.com
The LPG Cellu M6 Keymodule Gets FDA Clearance for Treating Lymphedema The FDA has just given the Class 1 Cellu M6 Keymodule, manufactured by LPG, Inc. (the world leader in connective tissue technology), full FDA clearance for treating Lymphedema. For_Immediate_Release:
Miami, FL – According to the World Health Organization,
Lymphedema afflicts hundreds of millions worldwide. Of
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these, the US Department of Health and Human Services
estimates more than 300 million are American. Variousforms of massage are used to treat this painful condition,
but none really have enough consistency or depth-of-
action to produce results. But now one does. The Food and
Vetenskapligt bevisat resultat! LPG-Endermologie
Drug Administration (FDA), has just given the Class 1 Cellu
M6 Keymodule, manufactured by LPG, Inc. (a medical
device company renowned as the world leader in
connective tissue technology), full FDA clearance for
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Lymphedema. The new claims are as follows:
• Reduction of secondary Lymphedema of the arm (SLA)
post mastectomy (RX only)• Improvement of secondary Lymphedema (RX only)
• Improvement of lymphatic circulation in the treated area (RX only)
For this FDA clearance, LPG presented well-documented, scientifically proven clinical results showing the
Technology’s efficacy on the body’s circulatory, anti-edematous and dermatrophic systems. Along with these
published studies, multimodal clinical studies examining the efficacy and durability of the traditional ManualLymphatic Drainage (MLD) and Compression Bandaging (CB) versus the non-invasive LPG Treatment were
conducted by Neil Piller, M.D., Professor for Lymphology at the Lymphedema Assessment Clinic of Flinders
University Medical Center in South Australia.
Michel Van Welden, the Chief Executive Officer of Techno-Derm (LPG’s exclusive US distributor), explains, "Dr.
Piller’s research demonstrates that LPG Technology offers an all-inclusive, standardized therapy for SLA pathology –with greater consistency, efficacy and faster results than MLD – which confirms that LPG devices are essential for
The research concluded that the LPG Treatment showed significant decreases in perometry (18%), bio-impedance
(23.5%), and tissue softening in half the time as the MLD control group and with a sustained effect. What’s that
mean? That LPG’s FDA cleared Cellu M6 Keymodule presents a lastingly effective solution for millions ofLymphedema sufferers around the world. Lymphedema occurs whenever lymph nodes have been damaged - so
although this study examines the Cellu M6 Keymodule’s treatment of mastectomy Lymphedema – it’s
also ideal for Lymphedemas resulting from lumpectomies, radiation treatments and many other procedures.
Company Information:LPG Technology is marketed and distributed by Techno-Derm, LLC, (DBA: LPG America), 10800 Biscayne Blvd.,
Ste. 850 in Miami, Florida. For more on LPG treatments and LPG’s FDA-cleared , visit
To view a copy of Piller’s study, learn more about LPG’s FDA Lymphedema claims or schedule an interview with a
http://www.free-press-release.com/news/200812/1229457538.html
The LPG Cellu M6 Keymodule Gets FDA Clearance for Treating Lymphedema - Free-Press-Release.com
To view a copy of Piller’s study, learn more about LPG’s FDA Lymphedema claims or schedule an interview with aCompany representative, please contact Rebecca Hausen at 305-335-8696 or by email [email protected].
For more information:
3500 Coral Way, Ste. 1002 Miami, FL 33145 Representing www.cellum6.com
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