Actuated Medical, Inc. is one of 16067 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Actuated Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100, GripTract-GI Endoscopic Tissue Manipulator Lower GI Models, GripTract-GI Endoscopic Tissue Manipulator
10
Total
10
Cleared
0
Denied
Actuated Medical, Inc. has 10 FDA 510(k) cleared gastroenterology & urology devices. Based in Bellefonte, US.
Latest FDA clearance: Oct 2025. Active since 2012.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Actuated Medical, Inc.
10 devices
Cleared
Oct 31, 2025
GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100
Gastroenterology & Urology
211d
Cleared
Oct 04, 2024
GripTract-GI Endoscopic Tissue Manipulator Lower GI Models
Gastroenterology & Urology
59d
Cleared
Nov 03, 2023
GripTract-GI Endoscopic Tissue Manipulator
Gastroenterology & Urology
186d
Cleared
Oct 31, 2022
IO Needle Safety Sheath
General Hospital
217d
Cleared
Dec 04, 2020
TubeClear System
Gastroenterology & Urology
267d
Cleared
Jun 29, 2018
TubeClear System
Gastroenterology & Urology
309d
Cleared
Nov 30, 2016
TubeClear Control Box and Clearing Stem
Gastroenterology & Urology
26d
Cleared
Aug 16, 2013
TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS)
Gastroenterology & Urology
123d
Cleared
Dec 20, 2012
TUBE-CLEAR, CONTROL BOX (COMPONENT OF TUBECLEAR), CLEARING STEM (COMPONENT OF...
Gastroenterology & Urology
22d
Cleared
Jun 13, 2012
TUBECLEAR
Gastroenterology & Urology
15d