Medical Device Manufacturer · US , Ann Arbor , MI

Auxilium Biotechnologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026

Total

Cleared

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) cleared devices by Auxilium Biotechnologies, Inc.

1 devices

1-1 of 1