DistributorLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled 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 13, 2026, FDA's public records list Nissho Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 4, 1997: NIPRO ARTERIAL & VENOUS BLOOD TUBING SET FOR HEMODIALYSIS.
| Mar 4, 1997 | NIPRO ARTERIAL & VENOUS BLOOD TUBING SET FOR HEMODIALYSISK954676 · KOC | 510(k) clearances |
| Jun 4, 1996 | NIPRO ARTERIAL VENOUS FISTULA NEEDLEK955182 · FIE | 510(k) clearances |
| Mar 28, 1996 | NIPRO SAFELET CATHK960051 · FOZ | 510(k) clearances |
| Jan 4, 1996 | NIPRO SCALP VEIN SET (DISPOSABL PSV SET)K955053 · FOZ | 510(k) clearances |
| Dec 7, 1994 | NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLESK944355 · FMF | 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
