Askorn

ASKORN more than 15 year experience in medical devices. Based on a strong experience in medical devices, the founder of Askorn was willing to give an opportunity to orthopedic surgeons to develop and materialize their ideas and concepts related to implants and instruments. Askorn is born and sets up near Rennes, Brittany. The quality management system established by Askorn obtains the ISO 9001 & ISO 13485 certifications by AB Certification. Askorn moves into larger premises in Cesson-Sévigné. Transfer of the ISO 9001 & ISO 13485 to the notified body SNCH. CE-marking of the first class IIb implantable device fully designed by Askorn. Askorn is registered with the FDA. First placing on the American market of an Askorn-designed medical device. Askorn’s skills evolve and lead to the CE-marking of three new implantable class IIb medical devices. Change in notified body: Askorn is now ISO 13485 certified by the French notified body LNE / G-MED.