Medical Device Manufacturer · US , Philedelphia , PA

Implanet, S.A. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 2012

Total

Cleared

Denied

Implanet, S.A. has 15 FDA 510(k) cleared orthopedic devices. Based in Philedelphia, US.

Last cleared in 2023. Active since 2012.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. 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 - Implanet, S.A.

15 devices

1-15 of 15

Madison Total Knee System

ISS-JAZZ Screw System and JAZZ CAP SP

JAZZ System, including JAZZ Band

JAZZ CLAW System (hooks and rods) and JAZZ CLAW connector

IMPLANET Spine System (ISS)

IMPLANET SPINE SYSTEM

Data Source

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

Last updated: May 13, 2026

Implanet, S.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Implanet, S.A.

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