Kerr Corporation - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Kerr Corporation has 32 FDA 510(k) cleared dental devices. Based in Newport Beach, US.
Latest FDA clearance: Jan 2026. Active since 2006.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kerr Corporation
32 devices
Cleared
Jan 07, 2026
ZenSeal Pro
Dental
118d
Cleared
Jan 12, 2023
Rainbow 360
Dental
115d
Cleared
Aug 31, 2022
SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow
Dental
121d
Cleared
Oct 11, 2019
Nexus Universal Self-Cure
Dental
121d
Cleared
Nov 07, 2018
OptiBond eXTRa Universal
Dental
89d
Cleared
Aug 08, 2017
Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated...
Dental
291d
Cleared
Jul 18, 2017
Demi Ultra
Dental
258d
Cleared
Feb 03, 2017
GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated...
Dental
144d
Cleared
Jan 13, 2017
GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated...
Dental
163d
Cleared
Dec 21, 2016
EndoVac Pure
Dental
112d
Cleared
Nov 07, 2016
P1145 Dental Restorative
Dental
88d
Cleared
Jun 30, 2016
Identic and KromaFaze Alginate Dental Impression Materials
Dental
134d