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Data / Medical devices / Greece / DMP Dental Industry S.A.

DMP Dental Industry S.A.: FDA-registered device maker in Markopoulo Attiki, Greece, 9 510(k) clearances

DMP Dental Industry S.A. is registered with the FDA (registration 3008966075) in Markopoulo Attiki, Greece. It lists 8 device types. The FDA files 9 510(k) clearances under its listings, the newest dated January 13, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3008966075
Address
Kalyvion Avenue Markopoulo Industrial Zone, Markopoulo Attiki, Greece, 19003
Owner or operator
DMP Dental Industry S.A. (10037473)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
July 18, 2011
Registered through
2026
Brand names listed
BONA-BITE, BONA-BITE Air, BONA-BITE Crystal Vision, BONASCAN BITE AIR, BONASCAN HEAVY, BONASCAN LIGHT, BONASCAN Light Extra, BONASCAN MONO and more

Devices it lists

DeviceProduct codeClassRoleSource
Agent, Tooth Bonding, ResinKLE2Contract manufacturer, Manufactureraccessdata.fda.gov
Crown And Bridge, Temporary, ResinEBG2Contract manufacturer, Manufactureraccessdata.fda.gov
Liner, Cavity, Calcium HydroxideEJK2Manufactureraccessdata.fda.gov
Material, ImpressionELW2Contract manufacturer, Manufactureraccessdata.fda.gov
Material, Impression Tray, ResinEBH1Contract manufacturer, Manufactureraccessdata.fda.gov
Material, Tooth Shade, ResinEBF2Contract manufacturer, Manufactureraccessdata.fda.gov
Sealant, Pit And Fissure, And ConditionerEBC2Contract manufacturer, Manufactureraccessdata.fda.gov
Syringe, Restorative And Impression MaterialEID1Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 13, 2026K253248Bright Cavity LinerEJKSubstantially EquivalentDmp Dental Industry S.A.accessdata.fda.gov
November 6, 2025K252469MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCAKLESubstantially EquivalentDmp Dental Industry S.A.accessdata.fda.gov
September 2, 2020K192830Bright Temporary C&BEBGSubstantially EquivalentDmp Dental Industry S.A.accessdata.fda.gov
September 28, 2012K121915BRIGHT RESTORATIVE MATERIALSEBFSubstantially EquivalentDmp, Ltd.accessdata.fda.gov
January 13, 2011K102836BONASIL A+ IMPRESSION MATERIALSELWSubstantially EquivalentDmp, Ltd.accessdata.fda.gov
December 3, 2010K102252DMP PIT & FISSURE SEALANTEBCSubstantially EquivalentDmp, Ltd.accessdata.fda.gov
November 23, 2010K102255DMP ETCHING GELEBFSubstantially EquivalentDmp, Ltd.accessdata.fda.gov
November 23, 2010K102254DMP SINGLE BONDINGKLESubstantially EquivalentDmp, Ltd.accessdata.fda.gov
November 19, 2010K102257NANOCERAM- BRIGHTEBFSubstantially EquivalentDmp, Ltd.accessdata.fda.gov

Compare with other makers

Updated January 13, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.