510(k) Report

FDA applicant

W. Edward Johansen

Los Angeles, CA1 decision1998–19980 recalls

FDA records 1 decision for W. Edward Johansen (Los Angeles, CA) in 1998: 1 510(k) clearance. All are in product code EIA (Unit, Operative 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 W. Edward Johansen’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for W. Edward Johansen since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — W. Edward Johansen 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?

  • EIAUnit, Operative 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.

  • K973410UltracamW. Edward Johansen · 19981cites it

What has FDA decided for it lately?

  • K973410UltracamW. Edward Johansen · 1998

The one decision as W. Edward Johansen →