Dentlight, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentlight, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ultrafast, Ultrafast Plus, Ultrafast Lite, FUSION Plus Curing Light
4
Total
4
Cleared
0
Denied
Dentlight, Inc. has 4 FDA 510(k) cleared medical devices. Based in Richardson, US.
Last cleared in 2021. Active since 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentlight, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentlight, Inc.
4 devices