Medical device makerLabelled 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 15, 2026, FDA's public records list Nemoto Kyorindo Co., Ltd. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 27, 2024: Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 27, 2024 | Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)K242212 · DXT | 510(k) clearances |
| Feb 7, 2018 | PRESS DUO elite, PRESS DUO elite AGK173450 · DXT | 510(k) clearances |
| Jun 30, 2014 | DUAL SHOT ALPHA 7K133189 · DXT | 510(k) clearances |
| Oct 29, 2010 | REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESSK092896 · DXT | 510(k) clearances |
| May 21, 2010 | SONIC SHOT GXK091734 · IZQ | 510(k) clearances |
| Dec 19, 2007 | DUAL SHOT ALPHAK071691 · DXT | 510(k) clearances |
| Aug 18, 2006 | CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHAK062168 · DXT | 510(k) clearances |
| Oct 17, 2005 | DUAL SHOT - CONTRAST DELIVERY SYSTEMK052633 · DXT | 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
