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Other examples: Product Innovation, Evidence and Regulatory Impact

A selection of additional cases — from creative and digital workflows to high-impact FDA regulatory milestones.

BLX Technology Integration

Integrated Roxolid® and SLActive® technologies into BLX and helped position the implant system within Straumann® ImmediaXy™ as a high-performance solution for immediate treatment protocols.

Straumann® ImmediaXy™ Ecosystem

Helped shape and position Straumann® ImmediaXy™ as an end-to-end ecosystem connecting data acquisition, treatment planning, surgery and restoration for efficient and predictable immediate treatment workflows.

Straumann® ProClean Cassette

Led cross-functional development of the Straumann® ProClean Cassette, translating the demanding requirements of major hospitals and Sterile Services Departments into a validated, high-spec solution for fully automated instrument reprocessing. The platform helped secure adoption across 45+ US VA hospitals and 4 Bundeswehr hospitals, opening substantial downstream implant business and contributing to 20% implant revenue growth.

SLActive® Evidence in Irradiated Patients

Recognised a critical interpretation barrier in long-term SLActive® evidence for head and neck irradiated cancer patients and engaged Prof. Nelson to develop a clinical clarification. Aligned Clinical, Medical and Regulatory Affairs teams around the evidence and used the resulting publication as a key submission document supporting the removal of IFU restrictions and enabling predictable implant-supported prosthetic rehabilitation for this high-risk population.

Compromised Patients: FDA Regulatory Milestone

Established medically compromised patients as a strategic evidence and differentiation platform for SLActive®, leading the evidence roadmap and aligning Clinical, Medical and Regulatory Affairs around patients with Type II diabetes and those previously irradiated in the head and neck. The programme culminated in a major Regulatory Affairs milestone: FDA-cleared removal of both populations from IFU cautions and precautions, creating a unique regulatory position for Straumann and addressing significant unmet needs — including predictable implant-supported rehabilitation following oral cancer.

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