Kuros Biosciences is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Kuros Biosciences - FDA 510(k) Cleared Devices
Recent clearances: MagnetOs Easypack Putty
1
Total
1
Cleared
0
Denied
Kuros Biosciences has 1 FDA 510(k) cleared medical devices. Based in Bilthoven, NL.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kuros Biosciences Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bruder Consulting & Venture Group as regulatory consultant.
FDA 510(k) Regulatory Record - Kuros Biosciences
1 devices