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., part of General ElectricLabelled 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 15, 2026, FDA's public records list Lunar Corp. with 29 510(k) clearances. The most recent is a 510(k) clearance dated Jul 10, 2000: PEDIATRIC REFERENCE DATA.
| Jul 10, 2000 | PEDIATRIC REFERENCE DATAK001812 · KGI | 510(k) clearances |
| Jul 6, 2000 | LUNAR REPORT GENERATOR IIK001756 · KGI | 510(k) clearances |
| Apr 14, 2000 | PRODIGY LATERAL VIEW SOFTWAREK000826 · KGI | 510(k) clearances |
| Dec 8, 1998 | PRODIGY TOTAL BODY SOFTWAREK983564 · KGI | 510(k) clearances |
| Dec 8, 1998 | ORCA-DX BONE DENSITOMETERK983724 · KGI | 510(k) clearances |
| Nov 18, 1998 | FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERSK983271 · KGI | 510(k) clearances |
| Nov 18, 1998 | FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETERK983269 · KGI | 510(k) clearances |
| Nov 18, 1998 | FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERSK983262 · 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
