Arrow International, LLC (A subsidiary of Teleflex, Inc.) - FDA 510(k...
4
Total
4
Cleared
0
Denied
Arrow International, LLC (A subsidiary of Teleflex, Inc.) has 4 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Latest FDA clearance: Mar 2025. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arrow International, LLC (A subsidiary of Teleflex, Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Arrow International, LLC (A...
4 devices
Cleared
Mar 14, 2025
Arrow™ Endurance™ Extended Dwell Peripheral Catheter System (EDC-00818)
General Hospital
113d
Cleared
Dec 20, 2024
Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620)
General Hospital
140d
Cleared
Aug 30, 2022
Arrow Stiffening Stylet
Cardiovascular
210d
Cleared
Aug 22, 2022
VPS Rhythm DLX Device with TipTracker Technology
General Hospital
195d