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The Grasshopper - A revolution in portable Vaporizer Technology What We Did The Grasshopper was born out of the need for a great portable vaporizer.Unsatisfied with what was on the market, we took our backgrounds in aerospace engineering and applied that knowledge to vaporizer design.Using the absolute best technology available, we’ve built the most powerful, durable, and discreet vaporizer on the market today.
vaporizer gwint 510Scroll down to learn more.A great vaporizer has a great feel.A mechanical power button, metal construction and perfect balance are all part of that experience.We spent weeks deciding on the perfect dimensions, and designed everything else around those limits.A machined stainless steel or titanium housing protects the device even in the most demanding conditions.Unlike plastic and aluminum which show wear after just a few years, the materials in the Grasshopper are designed for life.

A cutting edge, high-tech battery packs a ton of power into a small package.Custom sizing and chemistry ensure maximum run time.A simple external dial allows for precise temperature adjustment from 130°C-210°C (266°F-410°F).This level of control means that your herbs will never burn.A 45 watt heating element means that there is always power to spare, no matter how aggressive the user.Our goal of building a great portable vaporizer included a great price, ensuring that we beat the competition in every way.Design - Built to Last Quality workmanship, ease-of-use, and superior design are elements absent from many of today's consumer products.Its been on a long journey to build a vaporizer with all three.Delays and manufacturing issues caused our team lots of stress, but we never sought to compromise the design of the Grasshopper.You’ll find that the Grasshopper is familiar, stylish and durable.But most importantly, it provides unparalleled performance.Design Features Specifically designed for dry or loose-leaf herbs Easily accessible chamber and temperature dial User-replaceable battery Pure convection technology 5 second startup time 95% metal construction 14mm Diameter X 140mm Length (0.55in X 5.50in) The Grasshopper - Titanium Edition The Titanium Grasshopper is made with a 100% titanium exterior, adding greater durability and reducing weight over the Stainless version.

This makes it the lightest and most durable portable vaporizer ever built.Features Medical grade titanium Durable and scratch resistant exterior Reduced weight over the Stainless version Same powerful heating element Order Titanium The Grasshopper - Color Edition The Color Grasshopper is made from anodized titanium for a durable and vibrant color coating.When investigating possible coating choices, it became apparent that a high quality anodization was the only way to provide a great finish.This is just another example of how nothing was left to chance.Color Choices Dark Grey Bronze Purple Blue Green Order ColorVaporizers, vape pens, hookah pens, electronic cigarettes (e-cigarettes), and e-pipes are some of the many types of Electronic Nicotine Delivery Systems (ENDS).These products use liquid containing nicotine, as well as varying compositions of flavorings, propylene glycol, glycerin, and other ingredients.The liquid is heated into an aerosol that the user inhales.

Many ENDS are manufactured to look like conventional cigarettes, cigars, or pipes.Some resemble pens or other everyday items.Larger devices such as tank systems or mods bear little or no resemblance to cigarettes.On this page, you can find: Statistics about ENDS Use FDA Regulation of ENDS Manufacturing ENDS and E-Liquids Nicotine Warning Statement Retail Sales of ENDS, E-Liquids, or their Components or Parts Made or Derived from Tobacco Vape Shops That Mix E-Liquids or Modify Products Importing ENDS and E-Liquids Report Adverse Experiences and Product Violations In 2016, FDA finalized a rule extending our regulatory authority to cover all tobacco products, including vaporizers, vape pens, hookah pens, electronic cigarettes (E-Cigarettes), e-pipes, and all other ENDS.FDA now regulates the manufacture, import, packaging, labeling, advertising, promotion, sale, and distribution of ENDS.This includes components and parts of ENDS* but excludes accessories.

However, products marketed for therapeutic purposes (for example, marketed as a product to help people quit smoking) are regulated by the FDA through the Center for Drug Evaluation and Research (CDER).FDA recently proposed a rule clarifying the jurisdiction over tobacco products, drugs, and devices.*"Components" or "parts" include, among other things, software or an assembly of materials intended or reasonably expected alter or affect the tobacco product's performance, composition, constituents, or characteristics; or to be used with or for the human consumption of a tobacco product.For a full definition of ENDS components, parts, and accessories, please read the final rule Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act.Examples of components and parts of ENDS include, but are not limited to: Battery Safety Concerns in Electronic Nicotine Delivery Systems (ENDS) Public Workshop - April 19-20, 2017 May 22, 2017 - Submit public comments At any time, interested parties with relevant scientific data may also contact the FDA directly to request an informal meeting on ENDS battery safety concerns.

Also see: Tips to Help Avoid Vape Battery Explosions If you make, modify, mix, manufacture, fabricate, assemble, process, label, repack, relabel, or import ENDS, you must comply with these requirements for manufacturers.CTP's Office of Small Business Assistance can answer specific questions about requirements of small businesses and how to comply with the law.This office also provides online educational resources to help regulated industry understand FDA regulations and policies.Beginning in 2018, the product packages and advertisements of all newly-regulated covered tobacco products must bear the following warning statement: "WARNING: This product contains nicotine.Nicotine is an addictive chemical."If the tobacco product manufacturer submits a self-certification statement to FDA that the newly-regulated tobacco product does not contain nicotine (and that the manufacturer has data to support this assertion), then an alternate statement must be used on product packages and advertisements: “This product is made from tobacco.” You can find more information about nicotine warning statements in the final rule, Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act.

Order FDA Rules for ENDS Sales Flyer If you sell ENDS, e-liquids, or their components or parts made or derived from tobacco, please read this summary of federal rules that retailers must follow.Click on the flyer thumbnail image to order printed materials from CTP's Exchange Lab or to download a PDF to print yourself.You can find a list of retailer responsibilities for ENDS in the final rule Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act.In addition, our website offers more information on regulations, guidance, and webinars for retailers.If you operate a vape shop that mixes or prepares liquid nicotine or nicotine-containing e-liquids, or creates or modifies any type of ENDS, you may be considered a manufacturer.As a result, some vape shops may have legal responsibilities as both manufacturers and retailers of tobacco products.Please also see the draft guidance Interpretation of and Compliance Policy for Certain Label Requirement; Applicability of Certain Federal Food, Drug, and Cosmetic Act Requirements to Vape Shops.

Tobacco products imported or offered for import into the United States must comply with all the applicable requirements under the Federal Food, Drug, and Cosmetic Act (FD&C Act).You can find more information on the Importing and Exporting webpage.You can also learn more about the importation process in the FDA Regulatory Procedures Manual, Chapter 9, Import Operations and Actions.If you have questions about importing a specific tobacco product, please contact the FDA district into which your product will be imported (PDF - 406 KB).If you have experienced an unexpected health or safety issue with a tobacco product, you can report an adverse experience to FDA.Knowledge about adverse experiences can help FDA identify health or safety issues beyond those normally associated with product use.If you believe these products are being sold to minors, or you see another potential violation of the FD&C Act or FDA’s tobacco regulations, report the potential violation.You can read the adverse event reports for ENDS that were voluntarily reported to FDA at the FOIA Electronic Reading Room.