Teleflex Medical, LLC is one of 25982 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: OnControl Powered Bone Access Systems, Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture, Polyethylene
3
Total
3
Cleared
0
Denied
Teleflex Medical, LLC has 3 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Latest FDA clearance: Oct 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
3 devices