I just did a google search with custom date range, 1/1/01 thru 2/15/07, and it appears that there were some, but I might be misunderstanding what the products are. Maybe somebody with more of an understanding of it, could do the search and see what they think.
The FDA has addressed that too. Am I the only one who thinks this sounds dismissive?
"Additionally, FDA has determined that some e-cigarettes and other ENDS were manufactured in 2006 and commercially marketed in the United States in early 2007. In particular, we have identified an ENDS product that may have been on the market on February 15, 2007. This product may possibly be able to serve as a valid predicate for purposes of the SE pathway.
"The burden of demonstrating that a valid predicate exists rests with the manufacturer submitting a SE report. To facilitate the determination that a product is eligible to serve as a valid predicate, any individual who has evidence that an e-cigarette or other ENDS was commercially marketed in the United States on February 15, 2007, may submit a stand-alone grandfather submission to FDA (See final guidance, "Establishing That a Tobacco Product Was Commercially Marketed in the United States as of February 15, 2007" (79 FR 58358, September 29, 2014)).
(Based on FDA's experiences to date, and since stand-alone grandfather submissions are purely voluntary, FDA does not anticipate that many manufacturers will make such submissions, but this option is available.)"
"Lol!" says the FDA. "You can give it a try, but the process is very expensive, time consuming and there's only a minute chance you will succeed. How much money do you have?"
I'm sure the ENDS product they have identified is NJOY. They may have the money to make it through the quagmire, but it's still a cigalike.
http://dealbook.nytimes.com/2014/02...eceives-funding-valuing-it-at-1-billion/?_r=0