
Processing and assembly
Bonetto ensures high flexibility and customization through the use of standardized machines and modular structures, designed to integrate seamlessly with the customer’s specific applications.
The range includes manual workstations, special systems for assembly lines with variable cycle times, and fully automated production lines, characterized by high standards of reliability, efficiency, and technological innovation.
Automation Solutions
Bonetto standard platforms are engineered to allow rapid and effective customization, adapting the base structure to the customer’s specific assembly needs.
The high degree of modularity ensures consistent quality standards even in the event of production increases. Our range includes:
Every project begins with a detailed analysis
of the production process
We support our customers in defining the most suitable solution,
combining modularity and customization.
Processes
Bonetto Med-Tech solutions are designed to automate and optimize the various stages of production processes. From component feeding to assembly, screwdriving, bonding, and marking, each system is developed to ensure efficiency, precision, and operational continuity.

FEEDING &
HANDLING

ASSEMBLY & PRINTING

BONDING

SCREWDRIVING

LABELING, MARKING & TRANSPORT
Certifications and
Reference Standards
Our automated lines are developed in compliance with key regulatory standards and reference guidelines for the medical and pharmaceutical sectors. A structured design approach that guarantees reliability, traceability, and compliance.
Quality Management System certified according to international standards. It guarantees structured processes, full traceability, and a continuous improvement approach across all design and manufacturing stages
Our automated lines are designed and built in accordance with current European machinery safety regulations, ensuring reliability, operator protection, and full compliance for market placement.
Software development follows international standards for industrial automation programming. This approach ensures structured, modular, and easily maintainable code, simplifying future interventions and integrations.
Our solutions are developed in compliance with Good Manufacturing Practices (GMP), the essential benchmark for the medical and pharmaceutical sectors. The lines are designed for integration into controlled contamination environments (cleanrooms), up to ISO Class 5, 6, and 7.
Our automation systems are developed following GAMP 5 guidelines, which define the best practices for regulated environments. This ensures a structured approach to system design, documentation, and validation.





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