Medical Device Manufacturer · US , Alendale , NJ

Acuitive Technologies, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2021

Total

Cleared

Denied

Acuitive Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Alendale, US.

Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Acuitive Technologies, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026