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Data / Medical devices / Canada / Frontier Dental Supply Inc

Frontier Dental Supply Inc: FDA-registered device maker in Aurora Ontario, Canada, 12 510(k) clearances

Frontier Dental Supply Inc is registered with the FDA (registration 3045891668) in Aurora Ontario, Canada. It lists 7 device types. The FDA files 12 510(k) clearances under its listings, the newest dated May 5, 2011. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3045891668
Address
450 Addison Hall Circle, Unit 9-12, Aurora Ontario, Canada, L4G 7C7
Owner or operator
Frontier Dental Supply Inc (10095856)
Roles
Exporter to the US
First device listed
May 11, 2026
Registered through
2027

Devices it lists

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
May 5, 2011K111185RELYX LUTING PLUS AUTOMIXEMASubstantially Equivalent3M Espe Dental Productsaccessdata.fda.gov
May 12, 2010K100235FILTEK SUPREME ULTRA FLOWABLE RESTORATIVEEBFSubstantially Equivalent3M Companyaccessdata.fda.gov
February 15, 2008K073697TRANSBOND SUPREME ADHESIVEDYHSubstantially Equivalent3M Unitekaccessdata.fda.gov
August 2, 2002K022476RELYX RMGIPEMASubstantially Equivalent3M Companyaccessdata.fda.gov
September 10, 2001K012442MODIFICATION TO CLEARFIL SE BONDKLESubstantially EquivalentKuraray Medical, Inc.accessdata.fda.gov
October 8, 1999K9923263M CLINPRO SEALANTEBCSubstantially Equivalent3M Companyaccessdata.fda.gov
November 17, 1997K973262KETAC-FIL APLICAP PLUSEMASubstantially EquivalentEspe GmbH & Co. Kg.accessdata.fda.gov
July 18, 1996K9620653M VITREBOND LIGHT CURE GLASS IONOMER/BASEEMASubstantially Equivalent3M Companyaccessdata.fda.gov
March 20, 1992K920424SCOTCHBOND BRAND MULTI-PURPOSE ADHESIVE SYSTEMKLESubstantially Equivalent3M Companyaccessdata.fda.gov
August 11, 1988K882690IMPRINT VINYL POLYSILOXANE IMPRESSION MATERIALELWSubstantially Equivalent3M Companyaccessdata.fda.gov
March 1, 1988K875133CAVIT-WEBGSubstantially EquivalentEspe GmbH (Us)accessdata.fda.gov
March 25, 1985K844846ESPE KETAC-CEM RADIOPAQUEEMASubstantially EquivalentEspe GmbH (Us)accessdata.fda.gov

Compare with other makers

Updated May 5, 2011. 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.