Medical device makerLabelled 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 Rubicor Medical with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 15, 2007: RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537.
| May 15, 2007 | RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537K071048 · KNW | 510(k) clearances |
| Mar 9, 2007 | FLEXIBLE LOOP ELECTROSURGICAL ELECTRODEK070275 · GEI | 510(k) clearances |
| Nov 18, 2005 | RUBICOR MAGIC BREAST BIOPSY DEVICEK053151 · KNW | 510(k) clearances |
| Oct 6, 2005 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108K052506 · GEI | 510(k) clearances |
| Sep 17, 2003 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629K032584 · GEI | 510(k) clearances |
| Jan 29, 2003 | MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086K030049 · GEI | 510(k) clearances |
| Nov 19, 2002 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086K023601 · GEI | 510(k) clearances |
| Apr 5, 2002 | RUBICOR BREAST BIOPSY DEVICEK020047 · GEI | 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
