FirmLabelled 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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Toray Industries, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2022: INOUE BALLOON A.
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.
| Dec 18, 2022 | INOUE BALLOON AK220881 · OZT | 510(k) clearances |
| Dec 17, 2004 | TORAYGUIDE GUIDEWIREK042370 · DQX | 510(k) clearances |
| Sep 29, 2003 | TORAYSULFONE DIALYZER, BS-L SERIESK030050 · KDI | 510(k) clearances |
| Oct 15, 2001 | TORAYSULFONE DIALYZERK002512 · KDI | 510(k) clearances |
| Aug 25, 2000 | HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0LK994198 · KDI | 510(k) clearances |
| Jun 22, 1995 | FILTRYZERK942681 · KDI | 510(k) clearances |
| May 19, 1995 | FILTRYZER(TM)K935471 · FJI | 510(k) clearances |
| May 4, 1995 | FILTRYZERK940910 · FJI | 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
