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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Actuated Medical with 10 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 2025: GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100.
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.
| Oct 31, 2025 | GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100K251041 · FDS | 510(k) clearances |
| Oct 4, 2024 | GripTract-GI Endoscopic Tissue Manipulator Lower GI ModelsK242325 · FDF | 510(k) clearances |
| Nov 3, 2023 | GripTract-GI Endoscopic Tissue ManipulatorK231254 · FDF | 510(k) clearances |
| Oct 31, 2022 | IO Needle Safety SheathK220890 · FMI | 510(k) clearances |
| Dec 4, 2020 | TubeClear SystemK200646 · KNT | 510(k) clearances |
| Jun 29, 2018 | TubeClear SystemK172556 · KNT | 510(k) clearances |
| Nov 30, 2016 | TubeClear Control Box and Clearing StemK163092 · KNT | 510(k) clearances |
| Aug 16, 2013 | TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS)K131052 · KNT | 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
