United States Endoscopy Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
United States Endoscopy Group, Inc. has 92 FDA 510(k) cleared gastroenterology & urology devices. Based in Mentor, US.
Historical record: 92 cleared submissions from 1991 to 2020.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - United States Endoscopy Group, Inc.
94 devices
Cleared
May 21, 2020
gi-4000 Electrosurgical Generator
General & Plastic Surgery
274d
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
Oct 23, 2017
gi-4000 Electrosurgical Generator
General & Plastic Surgery
35d
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
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