Dentalez, Inc., Stardental Division is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentalez, Inc., Stardental Division - FDA 510(k) Cleared Devices
Recent clearances: Star E900 Electric System, Star E900 Handpiece Series
2
Total
2
Cleared
0
Denied
Dentalez, Inc., Stardental Division has 2 FDA 510(k) cleared medical devices. Based in Lancaster, US.
Latest FDA clearance: Jan 2026. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentalez, Inc., Stardental Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentalez, Inc., Stardental Division
2 devices