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.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- 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
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Tooth Bonding, Resin | KLE | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Crown And Bridge, Temporary, Resin | EBG | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Liner, Cavity, Calcium Hydroxide | EJK | 2 | Manufacturer | accessdata.fda.gov |
| Material, Impression | ELW | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Material, Impression Tray, Resin | EBH | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Material, Tooth Shade, Resin | EBF | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Sealant, Pit And Fissure, And Conditioner | EBC | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Syringe, Restorative And Impression Material | EID | 1 | Repackager or relabeler | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 13, 2026 | K253248 | Bright Cavity Liner | EJK | Substantially Equivalent | Dmp Dental Industry S.A. | accessdata.fda.gov |
| November 6, 2025 | K252469 | MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCA | KLE | Substantially Equivalent | Dmp Dental Industry S.A. | accessdata.fda.gov |
| September 2, 2020 | K192830 | Bright Temporary C&B | EBG | Substantially Equivalent | Dmp Dental Industry S.A. | accessdata.fda.gov |
| September 28, 2012 | K121915 | BRIGHT RESTORATIVE MATERIALS | EBF | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
| January 13, 2011 | K102836 | BONASIL A+ IMPRESSION MATERIALS | ELW | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
| December 3, 2010 | K102252 | DMP PIT & FISSURE SEALANT | EBC | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
| November 23, 2010 | K102255 | DMP ETCHING GEL | EBF | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
| November 23, 2010 | K102254 | DMP SINGLE BONDING | KLE | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
| November 19, 2010 | K102257 | NANOCERAM- BRIGHT | EBF | Substantially Equivalent | Dmp, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Agent, Tooth Bonding, Resin
- All makers of Material, Impression Tray, Resin
- All makers of Syringe, Restorative And Impression Material
- All makers of Crown And Bridge, Temporary, Resin
- All makers of Material, Impression
- All makers of Material, Tooth Shade, Resin
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.