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In order to bring this technology to the bedside OrthoSera has developed the hypACT™ device isolating a specific serum derivative (SPRF) from the patient in a closed system, which is then applied during a same-day-procedure. This product has now received market authorization in Europe through a certification process by TÜV Rheinland.
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"After the successful launch of BoneAlbumin™ as our first commercial product in the dental field late last year this is another important milestone for our company," comments Dr. Zsombor Lacza, CEO of OrthoSera GmbH. "Following market authorization we are now making our autologous hypACT™ inject device available for clinical use in order to further build on the strong preclinical results of our hyperacute serum technology."