About AQUAfilling

The popularity of fillings and techniques available for soft tissues has widened the scope of what can be achieved by creating body volume and shape. AQUAfilling® is a bulking substance that has been specially developed to improve minimally invasive volume, including facial contours and breast augmentation. It is well tolerated, with long-term predictable results. As patients continue to opt for unscheduled procedures, developing less invasive products is welcome.

AQUAfilling® is a hydrophilic biodegradable gel that is biocompatible.

AQUAfilling® offers a non-invasive and non-surgical way to make human tissues look more attractive and more natural.
AQUAfilling® is a hydrophilic gel that acts as a reservoir for normal physiological solution of 0.9% sodium chloride solution blocked in the matrix of a three dimensional space-based linear polyamide structural polymorphic structure. Due to its positive charge, the gel attracts soluble, negatively charged extracellular matrix molecules – collagen and elastin, thus ensuring long-lasting skin elasticity and resistance.

AQUAfilling is constantly expanding through product registration around the world.

AQUAfilling has a vast network of distributors located on every continent.
At present, AQUAfilling is pending patent registration in 27 countries, Trademarked in 25 countries.
AQUAfilling constantly strives to make further registrations and certifications.

Biomedica spol. s.r.o.
Technologický park Hořátev
289 13 Zvěřínek
Czech Republic

AQUAfilling® products and the manufacturing process performed according to CE standards (European Union compliance standards), Korean GMP (Good Manufacturing Process) standards, ISO 13485: 2012 standards. These are the highest international standards.

In other words, AQUAfilling® products are supported by an industry-leading manufacturing process and compliance with the EU and South Korea for verifiable, safe and harmonized standards.

AQUAfilling® is manufactured in accordance with the strictest methods of sterilization and control considered necessary by EU and KFDA leaders. The strict application of the sterilization, packaging and product safety tests before release is carried out by independent laboratories and by the personnel designated by the manufacturer.

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