510(k) Report

FDA applicant

Diagnostic Data, Inc.

Upland, CA1 decision2002–20020 recalls

FDA records 1 decision for Diagnostic Data, Inc. (Upland, CA) in 2002: 1 510(k) clearance. All are in product code EKZ (Unit, Electrosurgical, And Accessories, Dental). No recall is linked to its devices.

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

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Diagnostic Data, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diagnostic Data, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diagnostic Data, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EKZUnit, Electrosurgical, And Accessories, Dental1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K020080Bonart Art-E1 Electrosurgery UnitDiagnostic Data, Inc. · 20021cites it

What has FDA decided for it lately?

  • K020080Bonart Art-E1 Electrosurgery UnitDiagnostic Data, Inc. · 2002

The one decision as Diagnostic Data, Inc. →

Other applicant names beginning “Diagnostic”

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

Diagnostic Products Corp. 324Diagnostic Systems Laboratories, Inc. 94Diagnostic Chemicals, Ltd. (Usa) 77Diagnostic Reagents, Inc. 66Diagnostic Chemicals, Ltd. 66Diagnostic Hybrids, Inc. 37Diagnostic Technology, Inc. 28Diagnostic Solutions, Inc. 26Diagnostic Ultrasound Corp. 16Diagnostic Systems 14Diagnostic Reagent Tech. 10Diagnostic Specialties 8