Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Belmont Equipment Corp. with 12 510(k) clearances. The most recent is a 510(k) clearance dated May 17, 2000: BELMONT UNIT, MODEL 2000 SERIES.
| May 17, 2000 | BELMONT UNIT, MODEL 2000 SERIESK000799 · EIA | 510(k) clearances |
| Jan 12, 1999 | BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIESK983661 · EIA | 510(k) clearances |
| Dec 23, 1996 | BELRAY/MODEL 096, DENTAL INTRAORAL X-RAYK963699 · EHD | 510(k) clearances |
| May 23, 1990 | PANORAMIC MODEL X-CALIBER X-RAYK900681 · EAP | 510(k) clearances |
| Dec 7, 1987 | MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAYK874238 · EHD | 510(k) clearances |
| Mar 25, 1987 | BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75K870300 · KPR | 510(k) clearances |
| Apr 24, 1986 | NEW BELMONT MODEL, MC-5 DENTAL, INTRAORAL X-RAYK861328 · EAP | 510(k) clearances |
| Jun 5, 1985 | BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RADK852019 · EAP | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
