Dentalez Group, Stardental Division is one of 20668 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentalez Group, Stardental Division - FDA 510(k) Cleared Devices
Recent clearances: 430 SWL 45 AND 430 SW 45 HIGH-SPEED HANDPIECES, NUTORQUE PROGRAMMABLE ELECTRIC SYSTEM
2
Total
2
Cleared
0
Denied
Dentalez Group, Stardental Division has 2 FDA 510(k) cleared medical devices. Based in Lancaster, US.
Historical record: 2 cleared submissions from 2009 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentalez Group, Stardental Division Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dekra Certification B.V as regulatory consultant.
FDA 510(k) Regulatory Record - Dentalez Group, Stardental Division
2 devices