FDA applicant

Allied Advanced Technologies (Aat)

Oak Brook, IL1 decision1988–19880 recalls

FDA records 1 decision for Allied Advanced Technologies (Aat) (Oak Brook, IL) in 1988: 1 510(k) clearance. All are in product code LWF (Dilator, Nasal). 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, ear, nose and throat panel, where it files most

How often FDA has decided Allied Advanced Technologies (Aat)’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allied Advanced Technologies (Aat) since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Allied Advanced Technologies (Aat) by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Allied”

FDA records each applicant name separately; these may or may not be the same firm.

Allied Healthcare Products, Inc. 26 Allied Associates, Inc. 9 Allied Biomedical Corp. 9 Allied Instrumentation Laboratory 7 Allied Signal, Inc. 2 Allied Rubber Industries Sdn. Bhd. 2 Allied Photo Products Co., Inc. 1 Allied Hill Enterprises, Ltd. 1 Allied Dental Solutions 1 Allied Medical Technologies, Inc. 1 Allied Fisher Scientific 1 Allied Systems Co. 1

Allied Advanced Technologies (Aat)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allied”