Ultrasight, Inc. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Ultrasight, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UltraSight AI Guidance
1
Total
1
Cleared
0
Denied
Ultrasight, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rehovot, IL.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ultrasight, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Ultrasight, Inc.
1 devices