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 Stellartech Research with 11 510(k) clearances. The most recent is a 510(k) clearance dated Oct 13, 2006: STELLARTECH 100 COAGULATION SYSTEM.
| Oct 13, 2006 | STELLARTECH 100 COAGULATION SYSTEMK061544 · GEI | 510(k) clearances |
| Apr 12, 2005 | STELLARTECH COAGULATION SYSTEM 2, MODELS 1100C-115A AND 1100C-230AK050831 · GEI | 510(k) clearances |
| Nov 12, 2004 | STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230AK042909 · GEI | 510(k) clearances |
| Jun 14, 2004 | STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 AND 1100C-230K041383 · GEI | 510(k) clearances |
| Apr 1, 2004 | STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)K040240 · GEI | 510(k) clearances |
| Oct 6, 2003 | MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230)K032721 · GEI | 510(k) clearances |
| Aug 21, 2003 | MODIFICATION TO: STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115 & 100C-230K032452 · GEI | 510(k) clearances |
| Jul 29, 2003 | STELLARTECH COAGULATION SYSTEM, MODELS (1100C-115 & 1100C-230)K032062 · 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
