Ultimed Incorporated is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ultimed Incorporated - FDA 510(k) Cleared Devices
Recent clearances: UltiCare Disposable Pen Needles, ULTICARE SAFETY SYRINGE WITH REMOVABLE NEEDLE
2
Total
2
Cleared
0
Denied
Ultimed Incorporated has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Last cleared in 2021. Active since 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ultimed Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ultimed Incorporated
2 devices