Medical Device Manufacturer · US , Fall River , MA

Teleflex Medical - FDA 510(k) Cleared Devices

39 submissions · 39 cleared · Since 2003

39

Total

39

Cleared

0

Denied

FDA 510(k) cleared devices by Teleflex Medical Cardiovascular ✕

2 devices

1-2 of 2

Cleared Sep 18, 2024

Arrow® Nitinol Wire

Cardiovascular · 90d

Cleared May 05, 2006

INTRODUCER ASSEMBLY WITH ROTATOR LOCK

Cardiovascular · 67d