Augmenta, LLC - FDA 510(k) Cleared Devices

Augmenta, LLC has 1 FDA 510(k) cleared medical devices. Based in Houston, US.

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

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

510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.