Tangent Endoscopy, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tangent Endoscopy, LLC - FDA 510(k) Cleared Devices
Recent clearances: Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller
1
Total
1
Cleared
0
Denied
Tangent Endoscopy, LLC has 1 FDA 510(k) cleared medical devices. Based in Camden, US.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Tangent Endoscopy, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by TAG3 Engineering as regulatory consultant.
FDA 510(k) Regulatory Record - Tangent Endoscopy, LLC
1 devices