Värmländsk
chair manufacturing
for more than 35 years
We are a family-owned company and we are proud that for more than 35 years we have created chairs that have been internationally recognized for their comfort and ergonomic characteristics. All our manufacturing, from cutting, sewing, cladding and assembly, takes place in our factory in Sunne in Värmland.
In 2020, Support Design AB got a new owner, CEO Cecilia Gimmersta Stove. She brings new ideas and visions for office furniture at a time when many workplaces are rapidly changing.
"I am delighted to have been given the opportunity to acquire Support Design and continue to run the company in the family spirit it already has. I love the craftsmanship and am very much looking forward to further developing these premium chairs and making them even more accessible to a global market. My vision is to develop beautiful chairs that make us feel really good and that can contribute to an increasingly circular economy."
How do you feel at work?
These are our watchwords at Support Design. Every day we ask ourselves how we can help our customers to sit well and work creatively, and still go home with energy and a happy body. We have a long background in ergonomic thinking and the desire to make your working day easier. Sustainability is our focus, both in terms of how we manufacture our products in Värmland and how we make our bodies last long and stay happy at work.
What sets us apart from other manufacturers of task chairs is the unique seat and back of the Support chair, which was designed by Bruno Mathsson in the 1970s on our behalf. As the pioneering designer he was, he started from the needs and function of the human body to create health chairs you can work in all day. The product range also includes a broad portfolio of saddle chairs developed in-house.
Our products comply with the MDR - Medical Device Directive
Support Design's chairs are registered as medical devices and meet all the requirements of the EU Medical Device Regulation (MDR, EU 2017/745). The MDR is the legislation that regulates how medical devices are developed, manufactured and controlled within the EU. It sets high standards for safety, traceability and documentation to ensure that products are safe for use in healthcare and medical environments.
