Arrow International, LLC (A subsidiary of Teleflex, Inc.)

FDA Regulatory Profile

Arrow International, LLC (A subsidiary of Teleflex, Inc.) appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 14, 2025.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243599Arrow™ Endurance™ Extended Dwell Peripheral Catheter System (EDC-00818)March 14, 2025
K242281Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended DwelDecember 20, 2024
K220280Arrow Stiffening StyletAugust 30, 2022
K220363VPS Rhythm DLX Device with TipTracker TechnologyAugust 22, 2022