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FDA Regulations on Tanning Beds: What You Need to Know(2026)
Apr 10 ,2026

FDA Regulations on Tanning Beds: What You Need to Know(2026)

What is the New Regulation of the FDA for Tanning Beds?

In March 2026, the FDA made a U-turn on their policy to impose a total ban on tanning beds for minors across the country. This new policy is a move towards an approach that is less prohibitive and more informative about the risks involved. Upon examining comments from all stakeholders and expert opinion, the FDA came up with a policy to revise current policies and educate users about the dangers of using tanning beds.

The key updates in the FDA’s new approach include:

  1. Improved Warnings on Tanning Machines: The FDA has made it mandatory for tanning machines to display better warnings about the dangers associated with exposure to ultraviolet rays, such as the risk of developing skin cancer and early signs of aging.

  2. Educational Campaigns: The FDA stresses the need to educate the general public, especially adolescents, regarding the hazards of indoor tanning.

  3. State-Level Regulations: While the FDA has not implemented a federal ban, individual states still have the authority to impose their own restrictions on tanning bed use. This allows states to tailor policies based on local health needs and concerns.


Moreover, the FDA continues to regulate the tanning equipment and ensure that the companies follow stringent safety protocols. In addition, the FDA advises the use of other methods for achieving a tan without putting oneself at risk of harmful UV rays.


There is an official FDA notice showing the proposal was withdrawn, and it’s published in the Federal Register

What's a Tanning Bed?

A tanning bed is one of the most common ways through which individuals achieve a tan. Tanning beds, however, pose serious health hazards among them being the risk of developing skin cancer. For this reason, the U.S. Food and Drug Administration has always been at the forefront of regulation of tanning equipment. In this blog, I will discuss the role played by the FDA in regards to tanning beds, their past plans, and recent updates.



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What is the FDA’s Role with Tanning Beds?

As the Food and Drug Administration is accountable for regulation of various products, the use of tanning beds is also under its supervision as they are regarded as Class II medical devices. The FDA controls the quality of these devices as well as issues various warnings related to the potential danger that may occur from using tanning beds, such as skin cancer caused by UV radiation. 


In other words, the FDA's objective is to keep the public safe from any harm connected with the use of tanning beds.


FDA Radiation-Emitting Products and procedures

FDA Tanning Products


For further details on the FDA’s decision and the reasoning behind it, refer to the following articles:

https://www.npr.org/2026/03/19/nx-s1-5752430/fda-tanning-beds

https://www.nbcnews.com/health/cancer/fda-pulls-proposed-rule-teens-tanning-beds-rcna263976


Conclusion


The FDA’s regulation of tanning beds has gone through many changes throughout the years, considering both public health issues and industrial interests. Even though at one point, the FDA was proposing that tanning beds should be banned for children, they have now taken a new course by concentrating on making their use safer and educating people about the dangers of ultraviolet rays. The goal is to ensure consumer protection while not banning it completely. 


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