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Data / Medical devices / United States / Advantage Dental Products, Inc.

Advantage Dental Products, Inc.: FDA-registered device maker in Clarkston, MI, United States, 4 510(k) clearances

Advantage Dental Products, Inc. is registered with the FDA (registration 1833025) in Clarkston, MI, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 23, 2014. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number
1833025
Address
4498 Klais DR., Clarkston, MI, United States, 48348
Owner or operator
ADVANTAGE DENTAL PRODUCTS, INC. (1833025)
Roles
Manufacturer, Repackager or relabeler
First device listed
November 22, 1992
Registered through
2027
Brand names listed
GrindRelief Pro, Hemaseal & Cide, Hemaseal & Cide Unidose, MATRIXTEMP, Matrix Buttons, Therm Tray 1

Devices it lists

DeviceProduct codeClassRoleSource
Crown And Bridge, Temporary, ResinEBG2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Mouthguard, Over-The-CounterOBRUManufactureraccessdata.fda.gov
Tray, Impression, PreformedEHY1Manufactureraccessdata.fda.gov
Varnish, CavityLBH2Manufactureraccessdata.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 23, 2014K133037GRINDGUARDOBRSubstantially EquivalentGrind Guard Technologies, LLCaccessdata.fda.gov
August 4, 2004K041886PROVISOEBGSubstantially EquivalentScientific Pharmaceuticals, Inc.accessdata.fda.gov
November 17, 1999K990779HEMASEAL & CIDELBHSubstantially EquivalentAdvantage Dental Products, Inc.accessdata.fda.gov
July 13, 1990K900389TEMPORARY CROWN MATRIX BUTTONSEBGSubstantially EquivalentAdvantage Dental Products, Inc.accessdata.fda.gov

Compare with other makers

Updated January 23, 2014. 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.