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 Entech with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 3, 1989: GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG.
| Aug 3, 1989 | GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFGK891371 · KNT | 510(k) clearances |
| Jun 2, 1989 | ENTAINER(TM) ENTERAL FEEDING CONTAINERK890430 · KNT | 510(k) clearances |
| Dec 7, 1987 | ENTUBE-MEER AND MEER FEEDING TUBE BRIDLE SYSTEMK873343 · KNT | 510(k) clearances |
| Nov 2, 1987 | ENTECH ENTERAL PUMP AND SETK873444 · FRN | 510(k) clearances |
| Jun 9, 1987 | ENFUSE ENTERNAL ADMINISTRATION SET & PUMP SETK871019 · KNT | 510(k) clearances |
| Jul 18, 1986 | ENTUBE TM, ENTERAL FEEDING TUBEK861427 · KNT | 510(k) clearances |
| Jun 16, 1986 | TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETSK861552 · KNT | 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
