Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017858031

FEI Number

3017858031

Entity Name

KING-DEVICK TECHNOLOGIES, INC

City/State/Country

Oak Brook, IL, US

Establishment Address

2150 McDonald Drive Unit 1120, Oak Brook, IL 60523, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

King-Devick technologies, inc (Owner Number: 10079862)

Owner / Operator Contact Address

2150 McDonald Dr, Unit 1120, Oak Brook, IL 60523, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K173669

PMA Number

N/A

All Registered Proprietary Names

King-Devick Test KD Balance King-Devick Variable Contrast Sensitivity Acuity Chart King-Devick Balance MiHED

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXV	Apparatus, Vestibular Analysis	Unknown	Class U	N/A	2020-12-29

Official Correspondent

Steven Devick

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

King-Devick technologies, inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017858031. Last updated year: 2026. Please use registration number 3017858031 when referencing this establishment in official correspondence.