Auxilium Biotechnologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Auxilium Biotechnologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeuroSpan Bridge
1
Total
1
Cleared
0
Denied
Auxilium Biotechnologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Auxilium Biotechnologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Auxilium Biotechnologies, Inc.
1 devices