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Data / Medical devices / United States / B And D Dental Corporation

B And D Dental Corporation: FDA-registered device maker in West Valley City, UT, United States, 1 510(k) clearance

B And D Dental Corporation is registered with the FDA (registration 3008190898) in West Valley City, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 11, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3008190898
Address
2371 S Presidents Dr Ste E, West Valley City, UT, United States, 84120
Owner or operator
B and D Dental Corporation (10040144)
Roles
Manufacturer
First device listed
March 13, 2012
Registered through
2026
Brand names listed
Origin Beyond Plus, Origin Beyond Plus Hybrid, Origin Beyond Plus Mono, Origin Beyond Plus Multi, Origin Live

Devices it lists

DeviceProduct codeClassRoleSource
Powder, PorcelainEIH2Manufactureraccessdata.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
August 11, 2011K110719ORIGIN ZIRCONIAEIHSubstantially EquivalentB&D Dental Technologiesaccessdata.fda.gov

Compare with other makers

Updated August 11, 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.