premarket tobacco product applications and recordkeeping requirements Decisions of the FDA on applications: Changes in the number of unique devices liquids used by US adults who frequently use electronic nicotine delivery systems, 2020–2023 FDA Formalizes a Flavor-Specific PMTA

FDA Formalizes a Flavor Specific PMTA Framework as Youth Vaping Continues to Decline The Continuum of Risk FDA Seeks Comments on Premarket Tobacco Product Applications Proposed Rule Office of Advocacy February 10, 2026: Roundtable on Premarket Tobacco Product Application (PMTA) Submissions for Electronic Nicotine Delivery Systems (ENDS) Products 02 10 2026 FDA U.S. Today, FDA posted a list of over 6 million deemed new tobacco products for which a premarket application was submitted to FDA via the Premarket Tobacco Product Application (PMTA) pathway What is a PMTA? The FDA Process Explained J&J Consulting Group FDA Regulatory Compliance

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