510(k) Report

FDA applicant

Optiva Corp.

Mercer Island, WA1 decision1992–19920 recalls

FDA records 1 decision for Optiva Corp. (Mercer Island, WA) in 1992: 1 510(k) clearance. All are in product code JEQ (Toothbrush, Powered). 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 Optiva Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Optiva Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Optiva Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • JEQToothbrush, Powered1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K921773TX Electric ToothbrushOptiva Corp. · 19922cite it

What has FDA decided for it lately?

  • K921773TX Electric ToothbrushOptiva Corp. · 1992

The one decision as Optiva Corp. →