FDA applicant

Belmont Equipment Corp.

Somerset, NJ12 decisions1981–20000 recalls

FDA records 12 decisions for Belmont Equipment Corp. (Somerset, NJ) from 1981 to 2000: 12 510(k) clearances. Most are in product codes EAP (Unit, X-Ray, Intraoral) and EHD (Unit, X-Ray, Extraoral With Timer). 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 Belmont Equipment Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Belmont Equipment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Belmont”

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

Belmont Instrument Corp. 22 Belmont Medical Technologies 1

Belmont Equipment Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Belmont”