510(k) Report

FDA applicant

Sandstrom Trade & Technology, Inc.

Ontario L2n 7c5, CA2 decisions1988–19880 recalls

FDA records 2 decisions for Sandstrom Trade & Technology, Inc. (Ontario L2n 7c5, CA) in 1988: 2 510(k) clearances. All are in product code HAW (Neurological Stereotaxic Instrument). 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, neurology panel, where it files most

How often FDA has decided Sandstrom Trade & Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sandstrom Trade & Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sandstrom Trade & Technology, 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?

  • HAWNeurological Stereotaxic Instrument2decisions

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.

  • K881131The Laitinen Stereotactic SystemSandstrom Trade & Technology, Inc. · 19881cites it

What has FDA decided for it lately?

  • K881132Laitinen's Trigeminus StereoguideSandstrom Trade & Technology, Inc. · 1988
  • K881131The Laitinen Stereotactic SystemSandstrom Trade & Technology, Inc. · 1988

All 2 as Sandstrom Trade & Technology, Inc. →