Medical Device Manufacturer · US , Redmond , WA

Endogastric Solutions, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2007

Recent clearances: EsophyX Z+ Device with SerosaFuse Fasteners and Accessories, EsophyX Z, EsophyX2 HD, EsophyX2 HD Device with SerosaFuse Fasteners and Accessories, EsophyX Z Device with SerosaFuse Fasteners and Accessories

11
Total
11
Cleared
0
Denied

Endogastric Solutions, Inc. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Redmond, US.

Latest FDA clearance: Apr 2024. Active since 2007.

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 Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Endogastric Solutions, Inc.

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