I
Individual dental restorations for the patient are produced with scrupulous craftsmanship as custom-made products in conformity with the German Medical Devices Act in controlled, quality assured work cycles.

II
The quality goals for the product are assured in the production process by controlled compliance with the Association of German Dental Technicians' Guilds (VDZI) quality criteria for dental laboratory technology services.

III The dental restorations created in the master laboratory reflect the current status of dental technology in Germany. They are produced in compliance with the requirements of dental medicine to suit the customer’s specific requirements.

IV
The medical device is fabricated using materials bearing the European CE marking.

V
The dental prosthesis is a medical device and as a special and as a custom-made product complies with the basic requirements set out in Annex I of Directive 93/42/EEC of 14 June 1993.

VI
As a manufacturer of medical devices which as customised products remain in the patient’s mouth for decades, the master laboratory operates a sustainably integrated safety concept.
Particular attention is therefore devoted during manufacture to ensuring compliance with the legal regulations for occupational, health and environmental protection.