With a vision of independence from R&D to production, our company was founded in 2017 in South Tangerang, Indonesia. In 2019, we relocated our production facilities to Bogor Regency, Gunung Sindur District. With full support from the Ministry of Health, our product quality standards have met the requirements for a Medical Device Manufacturer through national CPAKB certification and international ISO 13485 certification. We adhere to ISO product testing standards for each product to ensure its quality.
Our initial R&D, production facilities, and production processes all conducted in Indonesia. As a manufacturer in the Medical Devices sector, particularly the dental industry, we hope to compete and complement the foreign products already available in Indonesia. We also hope to expand our sales internationally.
We are committed to continuing to innovate and offer high-quality dental materials, ensuring we remain a leader in the dental industry, particularly in Indonesia.
HEXA DENTAL Quality Management System has been certified according to the requirements of the ISO 13485:2016 regulation. ISO 13485 is an International Organization for Standardization (ISO) standard, that represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices. It is to guarantee the highest quality of products and their compliance with legal requirements and customer expectations.
Hexa Dental Indonesia participated in more than 20 exhibitions throughout Indonesia during 2024. These included exhibitions held in Jakarta, Tangerang, Medan, Surakarta, and many other cities.
Hexa Dental Indonesia continues to expand its reach by participating in major exhibitions. Our presence throughout Indonesia continues to grow year after year, with the goal of becoming a national-scale medical equipment supplier.
With the aim of becoming a national-scale medical supply company.
To become the market leader for local dental material products in Indonesia.
