EAO 2025 MONACO

The EAO – European Association for Osseointegration is one of the most influential international congresses in the field of implantology and bone regeneration. Each year, it brings together clinicians, researchers, and industry leaders from around the world to share evidence-based practices, discuss clinical protocols, and explore the latest developments in the discipline.
The 2025 edition will take place in Monaco from September 18–20, in partnership with the French Society of Periodontology and Oral Implantology (SFPIO), and will focus on a key topic for daily clinical practice: “The impact of time in implant dentistry.”

The program will include interactive sessions, live video broadcasts, and—for the first time—the presentation of the First Global Consensus for Clinical Guidelines in Implant Dentistry, a landmark document that will help define new treatment standards in the field.

Discover the Future of Regenerative Dentistry

Visit us at Booth D69 – Diaghilev Floor to discover our latest solutions in regenerative dentistry. Our team will be available throughout the congress to present our biomaterials, share clinical insights, and discuss how our technologies can support your daily practice.

Whether you are looking to deepen your knowledge, explore new treatment options, or simply connect with like-minded professionals, we look forward to welcoming you to our stand.

Our booth at EAO 2025 in Monaco will be more than just an exhibition space — it will be a tangible expression of our identity. The color pink, a signature of our brand, will take center stage, embodying our vision of regenerative dentistry that blends scientific precision with human sensitivity.

The stand’s design, carefully curated down to the finest detail, will reflect our philosophy: clean lines, high-quality materials, and a layout conceived to encourage interaction and dialogue. Every element, from the graphics to the interactive stations, has been designed to offer an immersive experience aligned with our core values.
We certify that the entire range of medical devices described above is CE marked and manufactured in accordance with the requirements of Directive 93/42 / EEC implemented in Italy with the DLGS. n. 46 dated 24-02-97 and subsequent amendments. The company operates in compliance with UNI EN ISO 9001 standards.
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