A unique solution for dental practices and laboratories.

Available even in the Small version for reduced diameters (3 - 3.5 mm), to make it easier to manage narrow interproximal spaces.

Key indications: For the correct location of the implant position in a virtualenvironment both from intraoral and laboratory scanning

Material: Grade 5 Titanium

Workflow: Digital

Warranty : 2 years

Perfectly scannable surface because it is designed both in terms of shape and colour to work with the operating system of the various scanners on the market. Shape tapered to the diameter of the implant platform to allow easy insertion into the oral cavity without interference from the gingival tissue. VScrew retained inside the component to minimise the diameter of the screwdriver insertion hole. The lateral laser marking allows easy identification of the correct implant connection. We advise against opacifying unless otherwise indicated for the correct use of the scanner. Can be reused and sterilised

Unique component for dental practices and laboratories. Available for over 500 implant platforms. Libraries available for all prostheses linked to in-house and inlab digital flows

Tailor-made customisation both of the component and the library

Our prosthetic components are a series of processes resulting from design, production and testing which have been perfected and tested over time in order to guarantee the production of compatible components which have the same features as the original components.

The core of the design stage lies in the accurate and systematic study of the production of the original implant companies, supported by the information obtained through standard tests to evaluate the fatigue resistance of the components, simulating and stressing how they behave when in use. The choice of fully biocompatible materials guarantees exceptional quality to the user and end patient, contributing to the success and durability of the prosthetic project.

The CE marking of the entire Gemini Line indicates the conformity of the medical devices produced and all the business processes involved, designed as part of a Quality System compliant with the ISO 13485:2016 standard.