FDA applicant

Aromacryl, LLC

Royal Oak, MI1 decision2002–20020 recalls

FDA records 1 decision for Aromacryl, LLC (Royal Oak, MI) in 2002: 1 510(k) clearance. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Aromacryl, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aromacryl, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aromacryl, LLC

Which product codes does it file in?

What has FDA decided for it lately?