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
6
Total
6
Cleared
0
Denied
Dentca, Inc. has 6 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Latest FDA clearance: Jul 2026. 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.
6 devices
Cleared
Jul 01, 2026
DENTCA Tru Flexible
Dental
58d
Cleared
Nov 17, 2022
Dentca Base Premium, Dentca Base Hi-Impact
Dental
316d
Cleared
Feb 05, 2020
DENTCA Crown and Bridge
Dental
127d
Cleared
Nov 22, 2017
DENTCA DENTURE Teeth
Dental
106d
Cleared
Mar 03, 2017
Dentca Denture Base II
Dental
221d
Cleared
Jul 21, 2015
DENTCA DENTURE BASE
Dental
272d