Dentalez Group, Stardental Division is one of 5171 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
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.
Dentalez Group, Stardental Division — FDA 510(k) Products and Clearance History
2 devices
Cleared
Sep 25, 2013
430 SWL 45 AND 430 SW 45 HIGH-SPEED HANDPIECES
Dental
215d
Cleared
Feb 18, 2009
NUTORQUE PROGRAMMABLE ELECTRIC SYSTEM
Dental
106d