Resources
Quality
FDA Registration
Aquila Bioscience have been successfully registered as a foreign manufacturing facility with FDA under Owner/ Operator Number 10074735
The ABD Wipe product is registered with FDA under device listing D405606.
Aquila Bioscience are now permitted to market and sell the ABD Device in the US market.
CE Mark
Path to CE mark is underway and is expected to be completed in 2021
Aquila Bioscience in the News
Reports
28th October 2020
Irish Company Develop Technology Proven to Remove 99.99% of Coronavirus from Human Skin
Aquila Bioscience has successfully proven that its breakthrough Pathogen Capturing Technology safely removes 99.99% of SARS-CoV-2 from human skin. This is the first time a nature inspired, safe and non-toxic technology that is free from all harmful chemicals, has been proven to remove COVID-19 with such efficiency. The results show that this novel technology is equally if not more effective as the highest performing chemical-based methods currently on the market but without any of the environmental or health problems.
8th June 2020
Aquila Bioscience is selected for EIC Accelerator Funding
Aquila Bioscience has developed revolutionary decontamination technology that helps protect people from dangerous pathogens and other viral infections like coronavirus. We are delighted to receive funding from EIC which allows us to substantially scale up production and deliver this technology more quickly to frontline and other workers in Ireland and across the globe. This technology will make it safer for people to return to work and help get Ireland’s economy moving again.
29th May 2020
Aquila Bioscience Registered with FDA
Aquila Bioscience have been successfully registered as a foreign manufacturing facility with FDA under Owner/ Operator Number 10074735
The ABD Wipe product is registered with FDA under device listing D405606.
Aquila Bioscience are now permitted to market and sell the ABD Device in the US market.
