For Manufacturers

The Dental Implant Registry welcomes collaboration with manufacturers to support the accurate recording, traceability, and real-world monitoring of implantable devices and related materials used in dental implant treatment, including dental implants, abutments, associated components, and bone grafting products.

Manufacturers are invited to submit product catalogues, updates, and supporting materials to help ensure product information is accurate, current, and consistently captured within the Registry.

Manufacturers may also contribute through appropriate advisory and committee processes, including the Manufacturer Advisory Group, by providing technical and industry input on product metadata, classification, terminology, and evolving product developments. This supports high-quality data capture, meaningful analysis, and effective post-market monitoring.

All contributions are provided within a structured governance framework. The Registry remains independently governed, with clear conflict of interest and confidentiality requirements. Manufacturers do not direct Registry analyses, reporting, or publication decisions.

Benefits for Manufacturers

• Supports accurate and consistent clinician product selection

• Improves product and material traceability across real-world care

• Contributes to post-market monitoring and surveillance

• Supports understanding of real-world product use and performance trends

• May inform product development and continuous improvement

• Helps ensure product information remains current and clinically relevant

• Enables contribution through structured advisory and committee involvement