02/04/2026
InGeneron is pleased to announce successful certification under the EU Medical Device Regulation (MDR) (EU) 2017/745.
CE Certification was achieved following a comprehensive review of our Technical Documentation and ISO 13485 Quality Management System.
This milestone reflects InGeneron’s long-standing commitment to quality, regulatory rigor, and patient safety, and supports our continued ability to serve physicians and patients across the European Union.
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