Allumin8, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allumin8, Inc. - FDA 510(k) Cleared Devices
Recent clearances: A8 INTEGR8™ Porous Pedicle Screws
1
Total
1
Cleared
0
Denied
Allumin8, Inc. has 1 FDA 510(k) cleared medical devices. Based in Springfield, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Allumin8, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Allumin8, Inc.
1 devices