Betadent Knowledge-Based Company

Selected as the National Exemplary Quality Unit in 2024

Betadent Company started its operations in 1983 with the production of acrylic polymer artificial teeth. By establishing new units, the company has expanded its production to include acrylic polymers and copolymers under the license of Akrosan Germany, as well as dental materials such as root canal sealers and impression materials under the license of Tradent Germany.

Laboratory Products

Betadent's laboratory products, with a focus on quality, efficiency, and durability, are an ideal choice for dental laboratories and professionals. These products significantly enhance the processes of prosthetic fabrication and restoration, providing a professional and satisfying experience for users.

Clinical products

Betadent's clinical products are designed with a focus on quality, efficiency, and ease of use to meet the professional needs of dentists. These products assist dentists in providing treatments with high precision and quality, ensuring patient satisfaction.

Accessory Products

These products are manufactured in compliance with international standards and under the license of reputable German companies. They assist dentists and laboratory technicians in providing services with greater precision and quality.

Specialized Consultation

Betadent offers specialized consultation services to provide better customer support, allowing clients to book and receive advice in the field of dental products. These services are available both online and in-person.

The company has obtained the CE mark. It is worth mentioning that the continuous and round-the-clock efforts of Betadent's Research and Development unit in achieving the organization's goals and entering international markets are commendable.

The studies were conducted as part of an approved research project, registered under the number 52269 in the Researchyār system of the Faculty of Dentistry at Tehran University of Medical Sciences. The research focused on examining physical properties (fluidity, solubility, radiopacity, layer thickness, setting time), cytotoxicity, and antimicrobial properties.

The CE mark makes export to Europe easier. The implementation of the ISO 13485 standard aims to harmonize requirements and enforce regulations for quality management systems specific to the medical device industry.

The development path aligns with increased sales, and exports to neighboring countries through the branches we have established there clearly demonstrate our capabilities in sales and marketing. Expanding these branches to European countries is a goal we are working towards achieving.