Manufacturer registered with FDA

DMP Dental Industry S.A.

Markopoulo, Greece. Lists 8 dental device types with FDA across 1 registered establishment, and holds 3 510(k) clearances as applicant.

FDA owner/operator10037473Contract manufacturerManufacturerRepacker / relabeler2 clearances in five years
Device types listed
8
Brands and models
44
510(k) clearances
32020–2026
Markets registered in
959 registrations outside the US
Establishments
1Greece
2020: 12025: 12026: 120102020

510(k) clearances per year, 2007–2026

Registered in 9 markets

Where regulators' registries name DMP Dental Industry S.A. as the manufacturer or the registration holder of a device.

All markets
United States: 8 device types listedEuropean Union: 15 registrationsCanada: 12 registrationsSerbia: 12 registrationsAustralia: 6 registrationsPeru: 6 registrationsTaiwan: 4 registrationsCosta Rica: 3 registrationsIsrael: 1 registrations
RegisteredHome: GreeceOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerDMP Dental Industry S.A.3 clearances2020–2026Below
European UnionEUDAMEDManufacturerDMP Dental Industry S.A.15—Pure Global AI
CanadaHealth CanadaRegistration holderDMP DENTAL INDUSTRY SA.122020–2021Pure Global AI
SerbiaALIMSManufacturerDMP DENTAL INDUSTRY S.A.122023–2026Pure Global AI
AustraliaTGAManufacturerDMP Dental Industry SA62019–2026Pure Global AI
PeruDIGEMIDManufacturerDMP DENTAL INDUSTRY S.A.D.M.P. DENTAL INDUSTRY S.A.62017–2023Pure Global AI
TaiwanTFDAManufacturerDMP DENTAL INDUSTRY S.A.42011–2015Pure Global AI
Costa RicaMinisterio de SaludManufacturerDMP DENTAL INDUSTRY S.A.3—Pure Global AI
IsraelAMARManufacturerDMP Dental Industry S.A.1—Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What DMP Dental Industry S.A. 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 compositesMaker
BRIGHT FLOW COREBRIGHT LIGHTBRIGHT LIGHT FLOWBRIGHT POSTERIORETCHING GELNANOCERAM-BRIGHTNANOCERAM-BRIGHT FLOW
2011
Pit and Fissure Sealant and ConditionerEBC · Class 2Sealants & varnishesMaker
BRIGHT FLOW COREBRIGHT LIGHTBRIGHT LIGHT FLOWBRIGHT POSTERIORNANOCERAM-BRIGHT FLOWPIT & FISSURE SEALANT
2011
Resin Tooth Bonding AgentKLE · Class 2Bonding agentsMaker
MagnaBond Universal, MagnaBond Universal DCA, MagnaBond SESINGLE BONDING
2011
Resin Temporary Crown and BridgeEBG · Class 2Temporary crown & bridge materialsMaker
BRIGHT TEMPORARY C&B
2020
Resin Impression Tray MaterialEBH · Class 1Impression traysMaker
TRAY ADHESIVE
2022
Restorative and Impression Material SyringeEID · Class 1Dental hand instrumentsLister
DMP MIXER DYNAMIC-5:1 380ml YELLOW (50)DMP MIXER T-1:1 2.5-10-D BROWN (50)DMP MIXER T-1:1 2.5-10-SW BLUE (50)DMP MIXER T-1:1 3.2-12-S LIGHT BLUE (50)DMP MIXER T-1:1 4.2-12-D YELLOW (50)DMP MIXER T-1:1 5.4-12-D PINK (50)DMP MIXER T-1:1 6.5-12-D TEAL (50)DMP MIXER T-4/10:1 3.2-16-S LIGHT BLUE/ORANGE (50)
2020
Calcium Hydroxide Cavity LinerEJK · Class 2—Maker
Bright Cavity Liner
2026
Impression MaterialELW · Class 2Impression materialsMaker
BONA-BITEBONA-BITE AirBONA-BITE Crystal VisionBONASCAN BITE AIRBONASCAN HEAVYBONASCAN LIGHTBONASCAN Light ExtraBONASCAN MediumBONASCAN MONOBONASCAN Putty
8 more
BONASIL A+ Alginate FreeBONASIL A+ HeavyBONASIL A+ LightBONASIL A+ LIGHT EXTRABONASIL A+ Light HTSBONASIL A+ MonoBONASIL A+ PuttyBONASIL A+ Regular
2011

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

510(k) clearances

Clearances on which FDA names DMP Dental Industry S.A. as the applicant.

Decided510(k)DeviceDevice type
13 Jan 2026K253248Bright Cavity LinerEJK Calcium Hydroxide Cavity Liner
6 Nov 2025K252469MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCAKLE Resin Tooth Bonding Agent
2 Sep 2020K192830Bright Temporary C&BEBG Resin Temporary Crown and Bridge

Also lists devices cleared under other names

DMP Dental Industry S.A. 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: Dmp, Ltd. (6).

Decided510(k)DeviceApplicantDevice type
28 Sep 2012K121915BRIGHT RESTORATIVE MATERIALSDmp, Ltd.EBF Resin Tooth Shade Material
13 Jan 2011K102836BONASIL A+ IMPRESSION MATERIALSDmp, Ltd.ELW Impression Material
3 Dec 2010K102252DMP PIT & FISSURE SEALANTDmp, Ltd.EBC Pit and Fissure Sealant and Conditioner
23 Nov 2010K102254DMP SINGLE BONDINGDmp, Ltd.KLE Resin Tooth Bonding Agent
23 Nov 2010K102255DMP ETCHING GELDmp, Ltd.EBF Resin Tooth Shade Material
19 Nov 2010K102257NANOCERAM- BRIGHTDmp, Ltd.EBF Resin Tooth Shade Material

Registered establishments

EstablishmentLocationWhat it does
DMP Dental Industry S.A.FDA reg. 3008966075Markopoulo Attiki, GreeceContract manufacturer, Manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10037473). 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.