Ultrasight , Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ultrasight , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Ness Ziona, IL.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ultrasight , Ltd. Filter by specialty or product code using the sidebar.
2 submissions have an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
2 devices