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Data / Medical devices / United States / King-Devick Technologies, Inc

King-Devick Technologies, Inc: FDA-registered device maker in Oak Brook, IL, United States, 1 510(k) clearance

King-Devick Technologies, Inc is registered with the FDA (registration 3017858031) in Oak Brook, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 2, 2018. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3017858031
Address
2150 McDonald Drive Unit 1120, Oak Brook, IL, United States, 60523
Owner or operator
King-Devick technologies, inc (10079862)
Roles
Manufacturer
First device listed
December 29, 2020
Registered through
2026
Brand names listed
KD Balance, King-Devick Balance, King-Devick Test, King-Devick Variable Contrast Sensitivity Acuity Chart, MiHED

Devices it lists

DeviceProduct codeClassRoleSource
Apparatus, Vestibular AnalysisLXVUManufactureraccessdata.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
April 2, 2018K173669K-D BalanceLXVSubstantially EquivalentKing-Devick Technologies, Inc.accessdata.fda.gov

Compare with other makers

Updated April 2, 2018. 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.