Dentca, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentca, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dentca Base Premium, Dentca Base Hi-Impact, DENTCA Crown and Bridge
5
Total
5
Cleared
0
Denied
Dentca, Inc. has 5 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2022. Active since 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentca, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The 510k Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dentca, Inc.
5 devices