Bonyf AG Achieves EU-MDR Class IIa Certification for PerioCream

bonyf AG, a subsidiary of Belgium-based bonyf NV, has received EU Medical Device Regulation (EU-MDR) Class IIa certification for its product, PerioCream. Certified by DEKRA Certification GmbH, this approval allows dental professionals globally to access this periodontal paste. PerioCream serves as a protective adjunct to scaling and root planing (SRP) treatments, isolating inflamed gingiva and reducing bacterial recolonization. The product's efficacy includes decreased bleeding and pain, enhancing patient comfort. Currently, bonyf is advancing US FDA certification, anticipating approval in early 2026.