510(k) Report

FDA applicant

King-Devick Technologies, Inc.

Oakbrook Terrace, IL1 decision2018–20180 recalls

FDA records 1 decision for King-Devick Technologies, Inc. (Oakbrook Terrace, IL) in 2018: 1 510(k) clearance. All are in product code LXV (Apparatus, Vestibular Analysis). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided King-Devick Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2018: 1
2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — King-Devick Technologies, Inc. by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LXVApparatus, Vestibular Analysis1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K173669K-D BalanceKing-Devick Technologies, Inc. · 2018

The one decision as King-Devick Technologies, Inc. →

Other applicant names beginning “King-Devick”

FDA records each applicant name separately; these may or may not be the same firm.

King Diagnostics, Inc. 41King Systems Corp. 18King & Spalding 7King Dental Corp. 2King'S Sunglass Corp. 2King Handy Five Corp. 2King Mfg. Co. 1King Tool, Inc. 1King'S Bay Intl., Inc. 1King Kondom Products, Inc. 1King I Tech Corporation 1