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Data / Medical devices / United States / Wisconsin Vision Associates Inc.

Wisconsin Vision Associates Inc.: FDA-registered device maker in Burlington, WI, United States, 1 510(k) clearance

Wisconsin Vision Associates Inc. is registered with the FDA (registration 3015700153) in Burlington, WI, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 7, 2017. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3015700153
Address
156 S Pine St, Burlington, WI, United States, 53105
Owner or operator
Wisconsin Vision Associates Inc. (10080674)
Roles
Repackager or relabeler
First device listed
February 18, 2021
Registered through
2027

Devices it lists

DeviceProduct codeClassRoleSource
Lens, Contact, (Disposable)MVN2Repackager or relabeleraccessdata.fda.gov
Lenses, Soft Contact, Daily WearLPL2Repackager or relabeleraccessdata.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
November 7, 2017K173086NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact LensesLPLSubstantially EquivalentVisioneering Technologies, Inc.accessdata.fda.gov

Compare with other makers

Updated November 7, 2017. 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.