Stericube, LLC - FDA 510(k) Cleared Devices

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

Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Hillring & Associates, Inc. as regulatory consultant.