G.N.S Neolaser , Ltd. is one of 474 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
G.N.S Neolaser , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: neoLaser Laser Surgery Fibers, neoV980 & neoV1470 Diode Lasers, NEOV DIODE LASER FAMILY
3
Total
3
Cleared
0
Denied
G.N.S Neolaser , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Caesarea, IL.
Latest FDA clearance: Mar 2025. Active since 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by G.N.S Neolaser , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - G.N.S Neolaser , Ltd.
3 devices