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 15, 2026, FDA's public records list Sarstedt and its 1 subsidiaries with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 25, 2023: Safety Lancet.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Sarstedt and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 25, 2023 | Safety LancetK222801 · FMK | 510(k) clearances |
| Jul 25, 2005 | SAFETY NEEDLEK051019 · JKA | 510(k) clearances |
| Sep 12, 2003 | SAFETY-MULTIFLYK032150 · FPA | 510(k) clearances |
| Sep 12, 2003 | S-MONOVETTE EDTA K2-GELK031359 · PJE | 510(k) clearances |
| Apr 14, 2003 | URINE MONOVETTE BORIC ACIDK024237 · JSM | 510(k) clearances |
| Mar 30, 2001 | SARSTEDT NEEDLE PROTECTORK003382 · FMI | 510(k) clearances |
| Jan 31, 1992 | HEMOPLUSK913622 · KHE | 510(k) clearances |
| Jan 30, 1984 | THROMBO PLUSK834527 · GGK | 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
