Neurolief , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Neurolief , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurolief , 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.
FDA 510(k) Regulatory Record - Neurolief , Ltd.
2 devices