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 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Norland Medical Systems with 18 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 2000: MULTI-RACIAL REFERENCE POPULATION FOR PDEXA AND DISCOVERY.
| Jun 20, 2000 | MULTI-RACIAL REFERENCE POPULATION FOR PDEXA AND DISCOVERYK993176 · KGI | 510(k) clearances |
| May 16, 2000 | APOLLO MULTI-RACIAL REFERENCE POPULATIONK993337 · KGI | 510(k) clearances |
| Nov 22, 1999 | XR 46 DXA (CENTRAL) BONE DENSITOMETER, MODEL XR 46K992125 · KGI | 510(k) clearances |
| Jun 12, 1998 | FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETERK980289 · KGI | 510(k) clearances |
| Jun 12, 1998 | FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERSK980569 · KGI | 510(k) clearances |
| May 20, 1998 | REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETERK980125 · KGI | 510(k) clearances |
| Feb 13, 1998 | NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERSK973459 · KGI | 510(k) clearances |
| Jan 29, 1998 | NORLAND MODEL PDEXA BONE DENSITOMETERK973104 · KGI | 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
