Teleflex Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teleflex Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Polyethylene
2
Total
2
Cleared
0
Denied
Teleflex Medical, LLC has 2 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Teleflex Medical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Teleflex Medical, LLC
2 devices