The line between wellness products and medical devices is getting messier by the minute. Think fitness trackers. Period pain relief devices. Meditation headbands. Blue light masks. Sleep tech. They look like lifestyle products. They’re sold in beauty halls. But depending on what they do and more importantly, what you say they do, they might fall squarely under medical device regulations.

On September 25, 2024, the Food Standards Agency (FSA) and Food Standards Scotland (FSS) issued important guidance on caffeine in food supplements. This new guidance aims to promote safe consumption and manufacturing practices for supplements containing high levels of caffeine.

For manufacturers, importers, and distributors of medical devices, understanding the difference between CE and UKCA markings is vital. These marks signify compliance with specific standards and ensure the safety and efficacy of medical products in their respective markets.