Gi Supply, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gi Supply, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Renova RP Centesis Pump, EverLift Submucosal Lifting Agent
2
Total
2
Cleared
0
Denied
Gi Supply, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mechanicsburg, US.
Last cleared in 2023. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gi Supply, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gi Supply, Inc.
2 devices