Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implants Systems, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2015

Total

Cleared

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) cleared devices by Aesculap Implants Systems, LLC

3 devices

1-3 of 3