Registered with FDA

The Atlanta Dental supply Company

Duluth, GA, United States. Lists 5 dental device types with FDA across 1 registered establishment.

FDA owner/operator10060749Repacker / relabeler
Device types listed
5
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What The Atlanta Dental supply Company currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Resin Tooth Shade MaterialEBF · Class 2Dental compositesLister
Admira Flow
2022
Pit and Fissure Sealant and ConditionerEBC · Class 2Sealants & varnishesLister—2022
Dental CementEMA · Class 2Dental cementsLister—2022
Resin Tooth Bonding AgentKLE · Class 2Bonding agentsLister—2022
Cavity VarnishLBH · Class 2Sealants & varnishesLister—2022

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Also lists devices cleared under other names

The Atlanta Dental supply Company lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Voco GmbH (5), S & C Polymer GmbH (1).

Decided510(k)DeviceApplicantDevice type
1 Aug 2014K141610FUTURABOND M+Voco GmbHKLE Resin Tooth Bonding Agent
21 Dec 2011K113444N-HYBRIDE-COMPOSITE LC FLOWVoco GmbHEBF Resin Tooth Shade Material
24 Jul 2008K080814VOCO PROFLUORID VARNISHVoco GmbHLBH Cavity Varnish
18 Jul 2001K011756ADMIRA FLOWVoco GmbHEBF Resin Tooth Shade Material
9 Feb 1999K984097DC-CORES & C Polymer GmbHEBF Resin Tooth Shade Material
25 Feb 1992K915618PROVICOLVoco GmbHEMA Dental Cement

Registered establishments

EstablishmentLocationWhat it does
THE ATLANTA DENTAL SUPPLY COMPANYFDA reg. 1013257Duluth, GA, United StatesRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10060749). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.