Nitiloop , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Nitiloop , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NovaCross CTO Microcatheter
4
Total
4
Cleared
0
Denied
Nitiloop , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Herzliya, IL.
Historical record: 4 cleared submissions from 2015 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nitiloop , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Boston Biomedical Associates, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Nitiloop , Ltd.
4 devices