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 14, 2026, FDA's public records list Ito Co. with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 5, 2021: D function.
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.
| May 5, 2021 | D functionK203525 · NUW | 510(k) clearances |
| Oct 26, 2011 | US-101L, US-103SK112520 · IMI | 510(k) clearances |
| Nov 24, 2008 | MODEL ES-130K081943 · BWK | 510(k) clearances |
| Aug 25, 2008 | TM-400K081247 · ITH | 510(k) clearances |
| Oct 9, 2003 | US-100 PORTABLE ULTRASOUND THERAPY UNITK032793 · IMI | 510(k) clearances |
| Jan 28, 2003 | SW-180 SHORTWAVE THERAPY UNITK022846 · IMJ | 510(k) clearances |
| Oct 20, 1999 | TRIO 300K990787 · IPF | 510(k) clearances |
| Sep 1, 1999 | TM-300 TRACTION SYSTEMK992545 · ITH | 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
