Inscope, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inscope, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Inscope, LLC has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 2 cleared submissions from 1999 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Inscope, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inscope, LLC
2 devices