510(k) Report

FDA applicant

Metalor Technologies USA

North Attleborough, MA4 decisions2001–20020 recalls

FDA records 4 decisions for Metalor Technologies USA (North Attleborough, MA) from 2001 to 2002: 4 510(k) clearances. Most are in product codes EJT (Alloy, Gold-Based Noble Metal) and EJH (Alloy, Metal, Base). 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 Metalor Technologies USA’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metalor Technologies USA since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Metalor”

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