The screws supplied with the Gemini prosthetic components are the result of a thorough study of the original counterparts. This process leads to the production of components fully compatible with both New Ancorvis and original parts.

Fatigue testing during the design phase, stringent raw material inspections, in-process testing, and final inspections (including Torque Testing) during production ensure the release of safe and reliable products. The use of fully biocompatible materials guarantees maximum safety and quality for both the clinician and the patient, contributing to the successful and long-lasting outcome of the prosthetic restoration.

The CE marking of the entire Gemini Line certifies the compliance of the medical devices produced and all related company processes, designed within a Quality Management System compliant with ISO 13485 standards.