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 Humboldt Products with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 3, 1984: DRUMTO STAPES PROSTHESIS.
| Jan 3, 1984 | DRUMTO STAPES PROSTHESISK832540 · ETB | 510(k) clearances |
| Dec 9, 1982 | STAINLESS STEEL PISTONSK823483 · ETB | 510(k) clearances |
| Jan 22, 1982 | TEKNA MED MYRINGOTOMY DISPOS-OTO KITK813616 · ETD | 510(k) clearances |
| Oct 2, 1981 | SURGICAL RETRACTOR & ELASTIC STAYS, DISPK812562 · GDG | 510(k) clearances |
| Nov 12, 1980 | OTOLOGICAL VENTILATION TUBESK802587 · ETD | 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
