Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller
Sep 2025
150d
Tangent Endoscopy, LLC
1
Total
1
Cleared
0
Denied
Tangent Endoscopy, LLC — FDA 510(k) Submissions
Tangent Endoscopy, LLC has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Choledochoscope And Accessories, Flexible/rigid . Use the specialty filter in the sidebar to narrow results.
1 devices