510(k) Report

FDA applicant

Advanced Aeromedical, Inc.

Great Neck,, NY1 decision1998–19980 recalls

FDA records 1 decision for Advanced Aeromedical, Inc. (Great Neck,, NY) in 1998: 1 510(k) clearance. All are in product code ELR (Post, Root Canal). 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 Advanced Aeromedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Aeromedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Aeromedical, 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?

  • ELRPost, Root Canal1decision

What has FDA decided for it lately?

  • K974649Bio-Post Dental Post SystemAdvanced Aeromedical, Inc. · 1998

The one decision as Advanced Aeromedical, Inc. →