United States Endoscopy Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: gi-4000 Electrosurgical Generator, Lariat, Hot/Cold Snare, Bio Guard Air/Water & Suction Valves
94
Total
92
Cleared
0
Denied
FDA 510(k) Regulatory Record - United States Endoscopy Group, Inc. Gastroenterology & Urology ✕
69 devices
Cleared
Apr 21, 2020
Lariat, Hot/Cold Snare
Gastroenterology & Urology
29d
Cleared
Sep 17, 2019
Bio Guard Air/Water & Suction Valves
Gastroenterology & Urology
47d
Cleared
Aug 01, 2019
AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System...
Gastroenterology & Urology
49d
Cleared
Nov 21, 2018
Roth Net Retriever Product Line
Gastroenterology & Urology
35d
Cleared
Sep 21, 2018
AquaShield System CO2
Gastroenterology & Urology
31d
Cleared
Jan 05, 2018
AquaShield System CO2- Fujifilm
Gastroenterology & Urology
38d
Cleared
Mar 10, 2017
AdvanCE capsule endoscope delivery device
Gastroenterology & Urology
87d
Cleared
Jan 06, 2017
Oracle EUS Balloon
Gastroenterology & Urology
24d
Cleared
Dec 16, 2015
AquaShield system CO2, AquaShield system-PENTAX
Gastroenterology & Urology
26d
Cleared
Oct 15, 2015
iSnare system-Lariat
Gastroenterology & Urology
85d
Cleared
Aug 25, 2015
BioGuard Air/Water Valve, BioGuard Suction Valve
Gastroenterology & Urology
98d
Cleared
Jul 30, 2015
Infinity ERCP Sampling Device
Gastroenterology & Urology
20d
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