FDA applicant

Bettini S.P.A.

Ormond Beach, FL1 decision2012–20120 recalls

FDA records 1 decision for Bettini S.P.A. (Ormond Beach, FL) in 2012: 1 510(k) clearance. All are in product code EIH (Powder, Porcelain). 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 Bettini S.P.A.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Bettini S.P.A. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Bettini S.P.A.

Which product codes does it file in?

What has FDA decided for it lately?