Gi Scientific, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gi Scientific, LLC - FDA 510(k) Cleared Devices
Recent clearances: ScopeSeal Duodenoscope Protective Device
2
Total
2
Cleared
0
Denied
Gi Scientific, LLC has 2 FDA 510(k) cleared medical devices. Based in Newbury, US.
Historical record: 2 cleared submissions from 2014 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gi Scientific, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lakeshore Medical Device Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Gi Scientific, LLC
2 devices