United States Endoscopy Group, Inc. (Us Endoscopy) 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. (Us Endoscopy) - FDA 510(k) Clear...
Recent clearances: Ultramatrix EUS Balloon
1
Total
1
Cleared
0
Denied
United States Endoscopy Group, Inc. (Us Endoscopy) has 1 FDA 510(k) cleared medical devices. Based in Mentor, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by United States Endoscopy Group, Inc. (Us Endoscopy) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - United States Endoscopy Group, Inc. (Us Endoscopy)
1 devices