# K253361: Teleport Glide Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: OrbusNeich Medical (Shenzhen) Co., Ltd.
- Decided: Apr 10, 2026 after 192 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K935425 (1994). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173799: NaviCross 0.018, Terumo Corporation (2018) Summary page 5.
- K110540: Terumo Support Catheter, Terumo Medical Corp. (2011) Summary page 5.
- K231044: R2P Navicross, Terumo Medical Corporation (2023) Summary page 5.

## Indications for use
Teleport Glide Microcatheter is indicated for guiding and supporting a guidewire within the peripheral vasculature, allowing for the exchange of guidewires and delivery contrast media into peripheral vascular.

Source page: https://510kreport.com/device/K253361
Methodology: https://510kreport.com/methodology