# Tangent Endoscopy, LLC

- Location (FDA's records): Camden, DE
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: FBN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K251170: Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller (Sep 12, 2025)

Source page: https://510kreport.com/company/tangent-endoscopy