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 Greiner Bio-OneLabelled 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 Greiner America with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 4, 1997: GREINER VACUETTE BLOOD COLLECTION TUBE.
| Jun 4, 1997 | GREINER VACUETTE BLOOD COLLECTION TUBEK971220 · JKA | 510(k) clearances |
| May 12, 1997 | GREINER VACUETTE BLOOD COLLECTION TUBEK971239 · JKA | 510(k) clearances |
| May 12, 1997 | GREINER VACUETTE BLOOD COLLECTION TUBEK971236 · JKA | 510(k) clearances |
| May 2, 1997 | GREINER VACUETTE BLOOD COLLECTION TUBEK971221 · GIM | 510(k) clearances |
| Sep 5, 1996 | GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3K960860 · JKA | 510(k) clearances |
| Aug 30, 1996 | GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATORK960858 · JKA | 510(k) clearances |
| Aug 30, 1996 | GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATORK960857 · JKA | 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
