Kurin, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kurin, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kurin Blood Culture Collection Set with Kurin Lock Technology, Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models M-21221, M-21223, D-21221, D-21223, T-21221, T-21223), Kurin PIV Blood Collection Set with High Pressure
3
Total
3
Cleared
0
Denied
Kurin, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Last cleared in 2023. Active since 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kurin, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Independent Consultant as regulatory consultant.
FDA 510(k) Regulatory Record - Kurin, Inc.
3 devices
Cleared
Apr 28, 2023
Kurin Blood Culture Collection Set with Kurin Lock Technology
General Hospital
416d
Cleared
Feb 04, 2020
Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button...
General Hospital
210d
Cleared
Jan 18, 2019
Kurin PIV Blood Collection Set with High Pressure
General Hospital
186d