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

0 new drug approvals and 4 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00818)510(k)Mar 14, 2025General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	Mar 14, 2025
Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00622); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00820); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00822)510(k)Dec 20, 2024General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	Dec 20, 2024
Arrow Stiffening Stylet510(k)Aug 30, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Aug 30, 2022
VPS Rhythm DLX Device with TipTracker Technology510(k)Aug 22, 2022General Hospital	General Hospital	510(k)Substantially Equivalent (Traditional)	Aug 22, 2022