DIP Dental Implant Parts is a regulated manufacturing facility that upholds stringent international

quality standards, prioritizing certification for its globally distributed products

. Our commitment to quality is unwavering, and we adhere to all European directives, including

the Medical Device Directive (93/42/EEC), as well as ISO 13485:2016 standards.

Our facility undergoes regular inspections and routine audits conducted

by international auditors to ensure continued compliance.

We are proud to be certified to operate within the USA, having

successfully secured FDA Medical Devices Registration,

and we have obtained FDA 510(k) approval for specific implant products.

These achievements reflect our substantial investment in maintaining

the highest levels of quality in our manufacturing processes.

At DIP Dental Implant Parts, we operate in accordance with the following

standards to guarantee the excellence of our products: