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 Medical Engineering and Development Institute with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 1990: WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SET.
| Aug 24, 1990 | WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SETK902477 · DYB | 510(k) clearances |
| Aug 23, 1990 | BYRD DILATOR SHEATH SET - TEFLONK902469 · DRE | 510(k) clearances |
| Aug 7, 1990 | BYRD STAINLESS STEEL DILATORK902502 · GCC | 510(k) clearances |
| Apr 17, 1990 | LIFE-LINE(TM) VASCULAR ACCESS SYSTEMK895030 · LJT | 510(k) clearances |
| Jun 23, 1989 | BYRD EXTRACTOR SETK893480 · GCC | 510(k) clearances |
| Mar 22, 1989 | LOCKING WIRE GUIDE STYLETK890820 · GAD | 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
