FDA applicant

Air Techniques, Inc.

Hicksville, NY18 decisions1995–20190 recalls

FDA records 18 decisions for Air Techniques, Inc. (Hicksville, NY) from 1995 to 2019: 18 510(k) clearances. Most are in product codes EIA (Unit, Operative Dental) and MUH (System, X-Ray, Extraoral Source, Digital). Its devices cite 6 predicates, 3 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

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Air Techniques, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2019

2007high 2 (2019) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Air Techniques, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?