Dentlight, Inc. is one of 16555 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, DENTLIGHT ORAL EXAM LIGHT KIT
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dentlight, Inc.
4 devices