We strive to provide products and services to exceed customers' expectations. Strongly focused on continuous improvement, we monitor and respond to needs, complying with all regulatory requirements.
We operate a quality management system that meets the requirements of ISO 13485 and 14001. Our products are CE-marked and certified in accordance with recognized medical device standards.
Össur works closely with its suppliers worldwide to evaluate, audit and encourage responsible corporate practices.
Certificates & Licences
FDA device listing
International Organization for Standardization
Information on CE markings
European Union information on CE markings