Vibrant, Ltd. - FDA 510(k) Cleared Devices
3
Total
2
Cleared
1
Denied
Vibrant, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Yokneam, IL.
Last cleared in 2023. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vibrant, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
3 devices