
bonyf AG receives the EU-MDR Certification Class IIa for PerioCream
Knokke-Heist (Belgium), 15 October 2025, 6:00 a.m.; bonyf NV (Euronext Paris Ticker: MLBON), a leader in dental consumer goods, professional dental consumables and dermatological solutions, announces today that its brand, PerioCream, a mucoadhesive formulation based on NitrAdine®, applied by dental professionals as an adjunct to Scaling & Root Planing (SRP) has been granted a certification as a Class IIa medical device according to Medical Device Regulation (EU) 2017/745 Annex IX Chapter I+III.
The certification, issued by DEKRA Certification GmbH, Germany, Notified Body (ID Number: 0124) on September the 17th, 2025, releases PerioCream Periodontal Paste to dental professionals and practitioners across the world.
The Medical Device Regulation (EU) 2017/745 is one of the world’s most robust health tech regulations, and it plays a vital role in ensuring medical devices meet the highest standards.
It has replaced the Medical Device Directive (MDD) and brings a series of important improvements to conformity assessment for medical devices with the scope to ensure the quality, safety, performance and reliability of medical devices placed on the European Market; strengthen transparency of information related to medical devices for consumers and practitioners; enhance vigilance and market surveillance of devices in use. DEKRA Certification GmbH based in Germany with worldwide presence, is the notified Body of bonyf AG. We got the MDR certification from DEKRA including PerioCream, based on the sampling plan for reviews of class IIa devices.
For the UK market, European CE marking is currently accepted until specified deadlines and product risk classification. A UKRP (UK Representative) was already designated, and UK resellers can contact bonyf AG to obtain more information.
For the US market, bonyf AG initiated the certification process with FDA and currently bonyf AG is on track with expected certification by the US FDA beginning 2026.
What is PerioCream?
PerioCream Periodontal Paste is an adjunct to scaling and root planing (SRP) treatment applied by dental professionals on the gum line. PerioCream Periodontal Paste acts as a protective barrier by isolating inflamed gingiva and irritated oral tissues to prevent bacterial recolonization, help reduce bleeding and enhance natural healing. The product is clinically proven to significantly reduce pain after SRP, enhance patient comfort and improve the overall SRP experience.
Annex to the EU Certificate no. 50537-60-00-02
Cureus Journal of Medical Science
European Institute for Medical Studies (EIMS), St. Julian’s, Malta
bonyf’s strengths
- Products with patented formulations
- Produced in Switzerland compliant with stringent international quality regulations
- Proven clinical efficacy
- Commercial presence in 37 countries
- Prospects for solid growth and rapid profitability
- A fast-growing oral and dental care market

About bonyf
Incorporated in 1979, bonyf specialises in the development, production and selling of cutting-edge oral & dental care products. Through its unwavering commitment to innovation and continuous improvement, bonyf makes a real difference to people suffering from dental and oral conditions. The Company has its R&D facilities in Liechtenstein (in the reputable “Dental Valley”), a production plant in Switzerland and distributes its product range in 37 countries worldwide. Benefiting from seven patent protected formulations and products developed in-house, bonyf expects strong future development, driven by the fast-growing oral and dental care market