Epilator Corporation Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared Notes Device Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K761049 Device Name … Continue reading “Epilator Corporation”
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IGIA Forever Gone Plus In the 1990s, New York based IGIA inundated the U.S. with their electric tweezer scam. Their misleading infomercials and hard-sell direct response ads were selling as many as 2 million units a year and cost U.S. consumers hundreds of millions of dollars. In 2000, IGIA moved into the "transcutaneous hair removal" … Continue reading “Forever Gone Plus by IGIA (WARNING!)”
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Dura Corporation Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared NotesDevice Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K772322 Device Name DEPILATORY, ELECTRONIC … Continue reading “Dura Corporation”
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Electronic Depilatory Co. Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared Notes Device Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K771575 … Continue reading “Electronic Depilatory Co.”
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Electro-Kinetic Manufacturing Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared Notes Device Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K770791 Device Name DEPILATOR, … Continue reading “Electro-Kinetic Manufacturing”
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Epco Hair Removal Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared Notes Device Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K760423 Device … Continue reading “Epco Hair Removal”
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Tony Monturo Tony Monturo Hate that Hair Tony’s web page about TE is titled "Transdermal Electrolysis – From Both Sides." Like most AHRS sales material, Tony mixes fact and fiction in a way that makes it all seem truthful. She starts with accurate information about hair physiology and the process of galvanic hair removal. Then … Continue reading “Tony Monturo (WARNING!)”
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An electric tweezer scam that branched out into “transdermal electrolysis” with an electrified Q-Tip. An earlier version of this company was owned by Ruth Ellen Morris and is discussed on the original AHRS page. It is currently owned by Sharon Spencer. American Hair Removal Sytstem should be avoided by all consumers. Company contact information American … Continue reading “American Hair Removal System – AHRS (WARNING!)”
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Berkowits School of Electrolysis, Inc. Berkowits School of Electrolysis was founded in 1978 by Barry Herman. In 1982, Mr. Herman began manufacture of the Berkowits 2200S epilator, a needle-type thermolysis device. The device was cleared by FDA in 1986 under Docket K860056. Contact information: Address: Berkowits School of Electrolysis, 107-25 Metropolitan Ave., Forest Hills 11375 … Continue reading “Berkowits School of Electrolysis, Inc.”
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Burke International Corporation Little is known about the manufacturer of this electric tweezer scam at the time of this writing. Contact information Address: Telephone: Fax: Contact: website: email: Available devices Epilator name FDA 510(k) Cleared Notes Device Classification Name EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE Regulation Number 878.5360 510(k) Number K952117 Device Name … Continue reading “Burke/Neutech”
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