Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of STERISLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list United States Endoscopy Group with 96 510(k) clearances. The most recent is a 510(k) clearance dated May 21, 2020: gi-4000 Electrosurgical Generator.
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 21, 2020 | gi-4000 Electrosurgical GeneratorK192265 · GEI | 510(k) clearances |
| Apr 21, 2020 | Lariat, Hot/Cold SnareK200745 · FDI | 510(k) clearances |
| Sep 17, 2019 | Bio Guard Air/Water & Suction ValvesK192059 · ODC | 510(k) clearances |
| Aug 1, 2019 | AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILMK191559 · FEQ | 510(k) clearances |
| Nov 21, 2018 | Roth Net Retriever Product LineK182909 · FDI | 510(k) clearances |
| Sep 21, 2018 | AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - FujifilmK182258 · FEQ | 510(k) clearances |
| Apr 19, 2018 | Ultramatrix EUS BalloonK180731 · ODG | 510(k) clearances |
| Jan 5, 2018 | AquaShield System CO2- FujifilmK173650 · FEQ | 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
