Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in DenmarkLabelled 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 Unoplast A/S with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 21, 1990: FEEDING TUBE.
| Dec 21, 1990 | FEEDING TUBEK896734 · FPD | 510(k) clearances |
| Nov 5, 1990 | NELATON-, FEMALE - OR TIEMANN CATHETERK896729 · KOD | 510(k) clearances |
| Nov 2, 1990 | UNOMETER 500K896732 · EXR | 510(k) clearances |
| Mar 30, 1990 | SUCTION CATHETER STRAIGHT/COUDEK896730 · BSY | 510(k) clearances |
| Mar 30, 1990 | OXYGEN CATHETERSK896731 · BZB | 510(k) clearances |
| Feb 1, 1990 | VACCONK896733 · KGX | 510(k) clearances |
| Sep 26, 1980 | DISARP ORIGINALK802248 · GAO | 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
