United States Endoscopy Group, Inc.

FDA Regulatory Profile

United States Endoscopy Group, Inc. appears in FDA public data with 0 recalls, 94 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 21, 2020.

Summary

Total Recalls
0
510(k) Clearances
94
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K192265gi-4000 Electrosurgical GeneratorMay 21, 2020
K200745Lariat, Hot/Cold SnareApr 21, 2020
K192059Bio Guard Air/Water & Suction ValvesSep 17, 2019
K191559AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILMAug 1, 2019
K182909Roth Net Retriever Product LineNov 21, 2018
K182258AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - FujifilmSep 21, 2018
K173650AquaShield System CO2- FujifilmJan 5, 2018
K172805gi-4000 Electrosurgical GeneratorOct 23, 2017
K163495AdvanCE capsule endoscope delivery deviceMar 10, 2017
K163492Oracle EUS Balloon; Oracle EUS latex balloon - Olympus Radial; Oracle EUS latex balloon - Olympus LiJan 6, 2017
K153362AquaShield system CO2, AquaShield system-PENTAXDec 16, 2015
K152035iSnare system-LariatOct 15, 2015
K151345BioGuard Air/Water Valve, BioGuard Suction ValveAug 25, 2015
K151889Infinity ERCP Sampling DeviceJul 30, 2015
K151197Lariat snareJul 6, 2015
K140315US ENDOSCOPY DISTAL ATTACHMENT CAPApr 4, 2014
K140405TORRENT IRRIGATION SYSTEMMar 12, 2014
K131598ANAL RECTAL OVERTUBEFeb 26, 2014
K133736ENDOSCOPIC SUTURE CUTTERJan 7, 2014
K133513MULTI-STAGE SNAREDec 20, 2013