Founded by the Peletti family in 1989, Overline is a leading company in the production and marketing of high-tech professional beauty equipment. 25 years of research and development, responsible management, technical expertise and experience that have given rise to high-performance, high-quality products. An all-Italian production that meets some fundamental requirements such as effectiveness, ease of use, safety and is supported by an efficient after-sales service.


The company, which has always been committed to the creation of equipment compliant with legislative standards, guarantees its own production with two certifications: TUV EN ISO 9001:2008 and ISO 13.485:2003. The equipment intended for the Italian market is produced according to the rigorous regulations in force and the standards imposed by the decree of the Ministry of Economic Development n. 110 of 12/05/2011 ‘Regulation for the implementation of art.10, paragraph 1 of law 01/1990, relating to electromechanical devices used for the activity of beauticians’.


Overline distributes its equipment in Italy and in all European countries as well as in Africa, Latin America, Mexico, Asia and Japan, for this reason, in the catalogue, the words used to define technologies and characteristics are those permitted at an international level and more commonly used.


Heartfelt thanks to customers, resellers, distributors and dealers for their collaboration over all these years, which has allowed Overline to gain an important position in the market.


Overline is a trademark of Technology srl, certified company always searching for quality and safety. Today, the three certifications ISO 9001: 2015, ISO 13485, ISO 45001:2018 show that the production chain complies with regulations and international standards required for the production of biomedical equipment, electro-aesthetics and cosmetics.

  • The certification of the Quality Management System ISO 9001: 2015, internationally recognized, ensures that the products comply with the management system required by the standard for design, production, sale, development and research.
  • The certification ISO 13485 relevant to the Quality Management System for Medical Devices, is a reference standard for the Quality Systems as part of the regulatory procedures governing the design, production and the marketing of Medical Devices.
  • The certification ISO 45001 is a standard for the assessment of health and safety of employees.