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