Aurolab - FDA 510(k) Cleared Devices

Aurolab has 4 FDA 510(k) cleared medical devices. Based in Madison, US.

Last cleared in 2022. Active since 2003. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Aurolab Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Allied Regulatory Consulting as regulatory consultant.