UC-CARE , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
UC-CARE , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Navigo Workstation 2.3 (FPRMC00039), Navigo Workstation Version 2.0
5
Total
5
Cleared
0
Denied
UC-CARE , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Washington, US.
Latest FDA clearance: Aug 2025. Active since 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by UC-CARE , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Gsap.
FDA 510(k) Regulatory Record - UC-CARE , Ltd.
5 devices
Cleared
Aug 07, 2025
Navigo Workstation 2.3 (FPRMC00039)
Radiology
155d
Cleared
Jan 16, 2018
Navigo Workstation Version 2.0
Radiology
110d
Cleared
Feb 06, 2017
UC-CARE NaviGo Workstation
Radiology
308d
Cleared
Nov 01, 2011
UC-CARE NAVIGO SYTEM
Radiology
592d
Cleared
Aug 10, 2009
UC-CARE WARMING SYSTEM
General & Plastic Surgery
126d