A New Milestone for SciVision - achieved certification under the European Union Medical Device Regulation (MDR).

A New Milestone for SciVision

As the aesthetic medical industry enters the MDR era, only a limited number of manufacturers worldwide have successfully achieved certification under the European Union Medical Device Regulation (MDR).

We are proud to announce that SciVision Biotech has officially obtained CE certification under the MDR framework for our Class III non-lidocaine dermal filler products. This achievement reflects our long-term commitment to product quality, patient safety, regulatory excellence, and international standards.

The MDR certification marks another important milestone in SciVision’s global development and further strengthens our dedication to providing safe, innovative, and high-quality medical aesthetic solutions to healthcare professionals and patients worldwide.