510(k) Report

FDA applicant

The Tova Company

Portland, OR2 decisions2017–20180 recalls

FDA records 2 decisions for The Tova Company (Portland, OR) from 2017 to 2018: 2 510(k) clearances. All are in product code LQD (Recorder, Attention Task Performance). Its devices cite 2 predicates, 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 The Tova Company’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2017: 12018: 1
2017high 1 (2017) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — The Tova Company by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LQDRecorder, Attention Task Performance2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K173915Test of Variables of Attention (T.O.V.A.)The Tova Company · 2018
  • K170082Test of Variables of Attention (T.O.V.A.) Version 9.0The Tova Company · 2017

All 2 as The Tova Company →