Aesculap Implants Systems, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesculap Implants Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: activL® Next Generation Instrumentation, CoreHip® System
3
Total
3
Cleared
0
Denied
Aesculap Implants Systems, LLC has 3 FDA 510(k) cleared medical devices. Based in Center Valley, US.
Last cleared in 2023. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Aesculap Implants Systems, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aesculap Implants Systems, LLC
3 devices