BOISE, Idaho - TelAve -- Lotus Vaping Technologies, LLC, an industry leader in the manufacture of premium e-liquids, is pleased to announce that it has filed with the U.S. FDA Premarket Tobacco Applications (PMTAs) for 9 of their open system e-liquid lines and that it has already received an acceptance letter from the FDA on its first product. The PMTAs cover a broad assortment of e-liquids including proprietary e-liquid flavors in varying nicotine strengths and sizes.

The product lines that have filed PMTAs with the FDA include Nomenon, Noms X2, Nomenon Ice, Nomenon Salts, All Day Vapes, LQiD, Teleos Pure, Lotus Originals and Exotics. This puts these Lotus e-liquid products into the next stage of the PMTA process where its applications are being reviewed by the FDA for acceptance for substantive scientific review. Lotus looks forward to working with the FDA as it reviews our submissions.

The Lotus brand e-liquid lines that have filed PMTAs represent a total of 79 unique flavor profiles in multiple strengths and sizes that are now going through the PMTA review process. Through these PMTA filings, Lotus will continue be able to offer a diverse selection of e-liquid products that will position the company as a premier manufacturer of premium e-liquids for years to come in the vapor industry.

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Lotus committed significant company resources to file comprehensive applications and views this as a vital step to offer products that vapor companies and consumers can trust and offer adult consumers a broad range of products that satisfy a wide variety of consumer preferences and serve as alternatives to combustible cigarettes.

About Lotus Vaping Technologies, LLC

Established in 2013, Lotus is a leading manufacturer and wholesaler of premium e-liquids in the United States providing a diverse range of vapor products for sale to adult consumers. Lotus is committed to responsible manufacturing processes and utilizes only the highest standards in its e-liquid production.

www.LotusVaping.com