Actuated Medical, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251041 | GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100 | FDS | 2025-10-31 | View |
| 510(k) | K242325 | GripTract-GI Endoscopic Tissue Manipulator Lower GI Models | FDF | 2024-10-04 | View |
| 510(k) | K231254 | GripTract-GI Endoscopic Tissue Manipulator | FDF | 2023-11-03 | View |
| 510(k) | K220890 | IO Needle Safety Sheath | FMI | 2022-10-31 | View |
| 510(k) | K200646 | TubeClear System | KNT | 2020-12-04 | View |
| 510(k) | K172556 | TubeClear System | KNT | 2018-06-29 | View |
| 510(k) | K163092 | TubeClear Control Box and Clearing Stem | KNT | 2016-11-30 | View |
| 510(k) | K131052 | TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS) | KNT | 2013-08-16 | View |
| 510(k) | K123659 | TUBE-CLEAR, CONTROL BOX (COMPONENT OF TUBECLEAR), CLEARING STEM (COMPONENT OF TUBECLEAR) | KNT | 2012-12-20 | View |
| 510(k) | K121571 | TUBECLEAR | KNT | 2012-06-13 | View |
No matching devices.
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