Uramix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Uramix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Uramix CuraWay Biopsy Needle
1
Total
1
Cleared
0
Denied
Uramix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lansdowne, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Uramix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Uramix, Inc.
1 devices