Denx Advanced Dental Systems is one of 506 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Denx Advanced Dental Systems - FDA 510(k) Cleared Devices
Recent clearances: IGI-SYSTEM, IGI-SYSTEM
2
Total
2
Cleared
0
Denied
Denx Advanced Dental Systems has 2 FDA 510(k) cleared medical devices. Based in M.P. Misgav, IL.
Historical record: 2 cleared submissions from 2003 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Denx Advanced Dental Systems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Denx Advanced Dental Systems
2 devices