Actuated Medical, Inc.
Actuated Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2025.
Top product codes for Actuated Medical, Inc.
Recent clearances by Actuated Medical, Inc.
- K251041 — GripTract-GI Endoscopic Tissue Manipulator Upper GI Model GT-GS100
- K242325 — GripTract-GI Endoscopic Tissue Manipulator Lower GI Models
- K231254 — GripTract-GI Endoscopic Tissue Manipulator
- K220890 — IO Needle Safety Sheath
- K200646 — TubeClear System
- K172556 — TubeClear System
- K163092 — TubeClear Control Box and Clearing Stem
- K131052 — TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS)
- K123659 — TUBE-CLEAR, CONTROL BOX (COMPONENT OF TUBECLEAR), CLEARING STEM (COMPONENT OF TUBECLEAR)
- K121571 — TUBECLEAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.