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Data / Medical devices / United States / DMV Corporation

DMV Corporation: FDA-registered device maker in Zanesville, OH, United States, 1 510(k) clearance

DMV Corporation is registered with the FDA (registration 1523955) in Zanesville, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 9, 1983. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1523955
Address
1024 Military RD., Zanesville, OH, United States, 43701
Owner or operator
DMV Corporation (1523955)
Roles
Manufacturer
First device listed
July 22, 1992
Registered through
2026
Brand names listed
DMV 45, DMV 8 MM Convex Stronghold Insert, DMV 8 MM Stronghold Extrahold Insert, DMV 9.5 MM Stronghold Large Insert, DMV CONTACT LENS REMOVER-INSERTER, DMV Classic, DMV Luma-Serta Plus, DMV Luma-Serter and more

Devices it lists

DeviceProduct codeClassRoleSource
Inserter/Remover Contact LensKYE1Manufactureraccessdata.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
March 9, 1983K830496DMV ANGLERKYESubstantially EquivalentDmv Contact Lens Co.accessdata.fda.gov

Compare with other makers

Updated March 9, 1983. 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.