Medical Device Manufacturer · US , Mentor , OH

United States Endoscopy Group, Inc. - FDA 510(k) Cleared Devices

94 submissions · 92 cleared · Since 1991

94

Total

92

Cleared

0

Denied

FDA 510(k) cleared devices by United States Endoscopy Group, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Jul 02, 1991

LAPAROSCOPIC VESSEL ARTICULATOR

Cardiovascular · 89d

Cleared Jul 02, 1991

LAPAROSCOPIC TROCAR

Cardiovascular · 89d