Medical Device Manufacturer · FR , Strasbourg

Axilum Robotics - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

Recent clearances: TMS-Cobot TS MV

1
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1
Cleared
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Denied

Axilum Robotics has 1 FDA 510(k) cleared medical devices. Based in Strasbourg, FR.

Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Axilum Robotics 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 - Axilum Robotics

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