ISO 13485 certification

The manufacturing facility at INterface Biomaterials is fully certified to ISO 13485, a comprehensive standard of quality management systems, specifically for Medical Device Manufacturers.

By earning this internationally recognized certification, we offer our customers and suppliers an additional level of confidence in our quality, reliability, and commitment to continuous improvement. INterface BIOmaterials’ ISO 13485 certification indicates that the highest standards are guaranteed, because we know that you depend on the quality of our products and services.


CE certification X-Spheres™

INterface BIOmaterials developed a proprietary new product for the embolization of uterine fibroids, named X-Spheres™. CE certification concerning the Medical Devices for embolization therapies (class IIB) was obtained in spring 2013.