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., part of Fujifilm HoldingsLabelled 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 Fujifilm Corporaton with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 27, 2023: FUJIFILM Endoscope Model EI-740D/S.
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.
| Jan 27, 2023 | FUJIFILM Endoscope Model EI-740D/SK221551 · FDS | 510(k) clearances |
| Jan 11, 2023 | Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500DK223295 · FDA | 510(k) clearances |
| Nov 10, 2022 | FUJIFILM Endoscope Model EB-710PK220957 · EOQ | 510(k) clearances |
| Dec 2, 2021 | FUJIFILM Video Laparoscope EL-R740M30K212950 · GCJ | 510(k) clearances |
| Jun 30, 2021 | Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0K203717 · GCJ | 510(k) clearances |
| Aug 27, 2020 | Synapse 3D Cardiac ToolsK200973 · LLZ | 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
