Teleflex Medical Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teleflex Medical Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Force Fiber Suture, Force Fiber White and White/Blue, White/Black, Blue, and White/Green sutures
3
Total
3
Cleared
0
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) Regulatory Record - Teleflex Medical Incorporated
3 devices