Medical Device Manufacturer · NL , Bilthoven

Kuros Biosciences B.V - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2017

Recent clearances: MagnetOs MIS, MagnetOs Putty, MagnetOs Granules

Total

Cleared

Denied

Kuros Biosciences B.V has 12 FDA 510(k) cleared orthopedic devices. Based in Bilthoven, NL.

Latest FDA clearance: May 2025. Active since 2017.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Compliance Solutions, Ltd., BAAT Medical Products B.V. and Mcra, LLC.

Kuros Biosciences B.V is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kuros Biosciences B.V

12 devices

1-12 of 12

MagnetOs Easypack Putty

MagnetOs Easypack Putty

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 29, 2026

Kuros Biosciences B.V - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kuros Biosciences B.V

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