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 14, 2026, FDA's public records list Genesis Industries with 17 510(k) clearances. The most recent is a 510(k) clearance dated Feb 18, 2000: ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WEL….
| Feb 18, 2000 | ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELLK994361 · MQK | 510(k) clearances |
| Feb 10, 1997 | EVERT-ITK962828 · HGY | 510(k) clearances |
| Apr 4, 1988 | NOVO VIVO MODEL #17140 AND #17135K880377 · GAA | 510(k) clearances |
| Feb 16, 1988 | NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPK880376 · GBS | 510(k) clearances |
| Jan 3, 1984 | C & B 40 PENTRO C & B40K833290 · EIS | 510(k) clearances |
| Jan 3, 1984 | SATIN CAST ECONOCASTK833287 · EIS | 510(k) clearances |
| Dec 29, 1983 | C & B 45K833278 · EIS | 510(k) clearances |
| Dec 29, 1983 | C & B 61 PENTRON C & B61K833289 · EIS | 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
