FDA Takes Action Against Reset Technology Corporation for Adulterated and Misbranded Dental Devices
The United States Food and Drug Administration (FDA) has taken action against Reset Technology Corporation for its ResetSmile Partial Denture Device and its at-home ResetSmile Impression Kit Device, which are adulterated and misbranded under the Federal Food, Drug, and Cosmetic Act. The ResetSmile Partial Denture Device is a removeable dental appliance used to replace missing teeth and the ResetSmile Impression Kit Device is an impression kit used to help make the removeable dental appliance. You can read the FDA action here: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/reset-technology-corporation-704828-06092025.