Magentiq Eye, Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Magentiq Eye, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Haifa, IL.
Latest FDA clearance: Apr 2026. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Magentiq Eye, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
4 devices