Adcura, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adcura, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices
1
Total
1
Cleared
0
Denied
Adcura, Inc. has 1 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Adcura, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
FDA 510(k) Regulatory Record - Adcura, Inc.
1 devices