📋 FDA Reference
Teleport Glide Microcatheter
OrbusNeich Medical (Shenzhen) Co., Ltd.
FDA Clearance Information
Pathway
510K
Number
K253361 ↗
Decision Date
April 10, 2026
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.