Acuitive Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acuitive Technologies - FDA 510(k) Cleared Devices
Recent clearances: Citregen Tendon Interference Screw and Citrelock
1
Total
1
Cleared
0
Denied
Acuitive Technologies has 1 FDA 510(k) cleared medical devices. Based in Alendale, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Acuitive Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Acuitive Technologies
1 devices