Data / Medical devices / Netherlands / Kuros Biosciences BV

Kuros Biosciences BV: FDA-registered device maker in Bilthoven Utrecht, Netherlands, 11 510(k) clearances

Name: Kuros Biosciences BV FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Kuros Biosciences BV is registered with the FDA (registration 3008147766) in Bilthoven Utrecht, Netherlands. It lists 1 device type. The FDA files 11 510(k) clearances under its listings, the newest dated May 23, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3008147766
Address: Professor Bronkhorstlaan 10 Building 48, Bilthoven Utrecht, Netherlands, 3723MB
Owner or operator: Kuros Biosciences BV (10054453)
Roles: Complaint file establishment, Manufacturer
First device listed: March 24, 2017
Registered through: 2026
Brand names listed: MagnetOs Easypack Putty, MagnetOs Flex Matrix, MagnetOs Granules, MagnetOs MIS, MagnetOs Putty

Devices it lists

Device	Product code	Class	Role	Source
Filler, Bone Void, Calcium Compound	MQV	2	Complaint file establishment, Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
May 23, 2025	K243474	MagnetOs MIS	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
June 27, 2024	K241212	MagnetOs Easypack Putty	MQV	Substantially Equivalent	Kuros Biosciences	accessdata.fda.gov
April 1, 2024	K240442	MagnetOs Putty	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
January 19, 2024	K232347	MagnetOs Granules	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
December 20, 2023	K230736	MagnetOs Putty	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
December 15, 2023	K233607	MagnetOs Easypack Putty	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
November 21, 2023	K233245	MagnetOs Flex Matrix	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
April 14, 2022	K213959	MagnetOs Flex Matrix	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
January 10, 2022	K213111	MagnetOs granules	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
September 2, 2021	K211201	MagnetOs Easypack Putty	MQV	Substantially Equivalent	Kuros Biosciences B.V	accessdata.fda.gov
February 24, 2017	K161859	MagnetOs	MQV	Substantially Equivalent	Xpand Biotechnology BV	accessdata.fda.gov

Compare with other makers

All makers of Filler, Bone Void, Calcium Compound

Updated May 23, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.