510(k) Report

FDA applicant

Texas Airsonics, Inc.

North Attleboro, MA1 decision1992–19920 recalls

FDA records 1 decision for Texas Airsonics, Inc. (North Attleboro, MA) in 1992: 1 510(k) clearance. All are in product code KOJ (Airbrush). 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 Texas Airsonics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Texas Airsonics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Texas Airsonics, Inc.’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?

  • KOJAirbrush1decision

Who builds on its devices?

Later devices cite its devices 4 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.

  • K921748Model 2000 Dental Air Abrasive SystemTexas Airsonics, Inc. · 19924cite it

What has FDA decided for it lately?

  • K921748Model 2000 Dental Air Abrasive SystemTexas Airsonics, Inc. · 1992

The one decision as Texas Airsonics, Inc. →