Medical Device Manufacturer · US , Mansfield , MA

Teleflex Medical Incorporated - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Teleflex Medical Incorporated has 3 FDA 510(k) cleared medical devices. Based in Mansfield, US.

Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Teleflex Medical Incorporated Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Teleflex Medical Incorporated

3 devices

1-3 of 3