Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Bio-One and its 1 subsidiaries with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Nov 19, 2024: VACUETTE SAFELINK, REF: 450210.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Greiner Bio-One and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 19, 2024 | VACUETTE SAFELINK, REF: 450210Class II · The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the protective rubber sleeve bunching up and not | Device recalls |
| 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
