Exclusive: Glas says FDA-authorized G2 vape includes age-gating technology

Mar.17
Exclusive: Glas says FDA-authorized G2 vape includes age-gating technology
Glas has confirmed to 2Firsts that its G2 device, which received a FDA Marketing Granted Order (MGO), incorporates age-gating technology. Based on currently public information, this means the FDA has granted an MGO to the first ENDS product confirmed to incorporate age-gating technology, validating 2Firsts’ earlier inference.

2Firsts

March 17, 2026

 

Glas Inc. has confirmed to 2Firsts that the device granted marketing authorization by the U.S. Food and Drug Administration (FDA) on March 12 (U.S. Eastern Time) is its Glas G2 platform and that it incorporates age-gating technology, meaning that, based on currently public information, the FDA has authorized the first electronic nicotine delivery system (ENDS) product confirmed to include such a feature.

 

In a message to 2Firsts, Kevin Higgins, chief operating and financial officer of Glas Inc., said the product that received the marketing granted order “is the Glas G2 device” previously discussed with 2Firsts and that it “does incorporate advanced, proven age-gating and counterfeit-detection technology.”

 

The confirmation validates 2Firsts’ earlier reporting on the platform behind the authorization.

 

On March 13, 2Firsts reported that the FDA had granted marketing authorization to a Glas device and a Blonde Tobacco pod, bringing the number of FDA-authorized ENDS products to 41. In a follow-up report published on March 14, 2Firsts reported that the FDA had updated the authorized product name to “Glas G2,”and, based on that change, inferred that the device receiving the marketing granted order likely corresponded to the Glas G2 platform previously described by the company as incorporating age-verification technology.

 

2Firsts will continue to monitor developments in the U.S. PMTA process.

 

Cover image generated by AI.

 


 

Further reading:

 

2FIRSTS | Special Report|FDA Revises Device Name in Glas Vape Authorization; Company Signals Optimism on Menthol, Flavored Pods
2FIRSTS | Special Report|FDA Revises Device Name in Glas Vape Authorization; Company Signals Optimism on Menthol, Flavored Pods
The FDA updated public records on the PMTA authorization of a Glas vape product, renaming “Glas G Device” to “Glas G² Device” and releasing the order letter detailing scientific review and marketing restrictions. Company disclosures suggest the platform may include age-verification technology. If confirmed, Glas G² could be the first vape with device-level age verification to receive an FDA MGO. Glas executives also said menthol and other flavored pods could gain authorization in the future.
www.2firsts.com

2FIRSTS | FDA Authorizes Glas Vape but Flavor Hopes Fall Short
2FIRSTS | FDA Authorizes Glas Vape but Flavor Hopes Fall Short
The FDA has added Glas products to its authorized electronic nicotine delivery systems (ENDS) list, granting Marketing Granted Orders (MGOs) to the Glas G DEVICE and a BLONDE TOBACCO pod. The decision expands the number of FDA-authorized ENDS products to 41, marking the first new authorization since Juul’s approvals in July 2025. However, widely anticipated non-tobacco flavored products were not approved.
www.2firsts.com

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TPB Q4 FY2025 Revenue Rises 29% to $121 Million; Modern Oral Business Up 266% Year Over Year
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Turning Point Brands, a U.S. nicotine and tobacco-related consumer products company, reported its fiscal 2025 fourth-quarter results: quarterly revenue was $121 million, up 29% year over year; adjusted EBITDA (Earnings Before Interest, Taxes, Depreciation and Amortization) was $30 million, up 14%. Net revenue from modern oral nicotine products was $41.3 million, up 266% year over year.
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