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EndoChoice

Medical device maker in United States, part of Boston Scientific. FDA records under 2 spellings of its name, each linked to the record.

  • 510(k) clearances: 27
  • Device recalls: 1

Latest Records

Newest first across sources; each opens the record
DateRecordSource
Aug 1, 2016Fuse Endoscopic System with FuseBox ProcessorK160275 · PEA510(k) clearances
Jun 27, 2016EndoChoice Water Bottle Cap Irrigation SystemK161482 · FEQ510(k) clearances
May 26, 2016Seal Single-Use Biopsy ValveK161167 · OCX510(k) clearances
May 19, 2016SmartStart Air/Water and Suction ValvesK160403 · ODC510(k) clearances
Feb 24, 2016EndoChoice Water Bottle Cap SystemK153588 · FEQ510(k) clearances
Feb 8, 2016EndoChoice Select Injection NeedleK151475 · FBK510(k) clearances
Dec 18, 2015Fuse 1C ColonoscopeClass II · The bending section of the device may partially separate from the insertion tube. Potential for tissue trauma.Device recalls
Dec 10, 2015Fuse Gastroscopy SystemK152182 · FDS510(k) clearances
Nov 3, 2015rescuenetK152580 · FDI510(k) clearances

Names and Identifiers

Appears as
Endochoice, Inc.EndoChoice, Inc.

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

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.