Stericube, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stericube, LLC - FDA 510(k) Cleared Devices
Recent clearances: SteriCUBE® Multiple Tray Sterilization Systems
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Stericube, LLC
1 devices