Endoscopic suture/plication system, gastroesophageal reflux disease (gerd)
FDA product code ODE · Class 2 · 8 devices · 118 reports · 1 deaths reported · 2 devices named in recalls
- EsophyX Z+ R2007Endogastric Solutions, Inc. · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)1 recall1 death69 reports
- SerosaFuse® Implantable Fastener Kit R2275Endogastric Solutions, Inc. · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)1 recall22 reports
- EsophyX2 HD R2005Endogastric Solutions, Inc. · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)11 reports
- EsophyX Z R2006Endogastric Solutions, Inc. · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)6 reports
- MUSE Endostapler 01Medigus Ltd · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)5 reports
- SerosaFuse®Merit Medical Systems, Inc. · Endoscopic suture/plication system, gastroesophageal reflux disease (gerd)3 reports
- EsophyX® Z+ AMerit Medical Systems, Inc. · Endoscopic suture/plication system, gastroesophageal reflux disease (gerd)1 report
- MUSE Staple Cartridge 02Medigus Ltd · Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)1 report