Encrypted transmission via SSL
To transfer your data, we use a secure server with SSL technology (Secure Socket Layer) with 128-bit encryption. In this way, your data is transmitted to us securely and unreadable for unauthorized persons.
3-Year guarantee on PrimeLOC attachments
The production of our PrimeLOC attachments is in accordance with strict quality control standards. As a testament to LASAK's world-class quality control, all our PrimeLOC attachments have a 100% satisfaction guarantee. This includes a 3-year guarantee on PrimeLOC attachments.
LASAK peace of mind lifetime guarantee
Before leaving our production plant in Mnichovo Hradiště, each of our products goes through a careful multi-level inspection using top brand measuring devices. All LASAK products are manufactured exclusively by our highly qualified employees.
We stand 100% behind the quality of our products. That’s why you have a lifetime guarantee from us on LASAK dental implants. We guarantee that, in the case of a loss or failure of an inserted LASAK implant we will replace the implant free of charge, including a matching cover screw or gingiva former and an abutment. The guarantee terms are described in more detail in the LASAK Guarantee.
All LASAK products bear the CE mark. It appears on many products traded on the extended Single Market in the European Economic Area (EEA). They signify that products sold in the EEA have been assessed to meet high safety, health, and environmental protection requirements.
Quality management systems
LASAK manufactures and markets medical devices of all classes, even those for the IIb and III risk classes. Production takes place in clean areas that are validated on an annual basis and fulfil the strict requirements of the EN ISO 14644 standard. LASAK complies with all requirements imposed by legislation as well as the requirements of its quality management system in compliance with the EN ISO 13485 standard and is a holder of QMS certificates (confirming that the management system guarantees quality). These are consistent with the European directives 93/42/EEC, 90/385/EEC and 98/79/EC.
The certificate according to EN ISO 13485:2016 standard covers the whole system of management of the organisation manufacturing or supplying medical devices and appropriate services.