Novoxel , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Novoxel , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Tixel i (TXLI0001), Tixel® 2 System, Tixel System
3
Total
3
Cleared
0
Denied
Novoxel , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Novoxel , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Regulatory Pathways Group, Inc.. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Novoxel , Ltd.
3 devices