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 expect to be completed in 2020
