Teleflex Medical - FDA 510(k) Cleared Devices

Teleflex Medical is an American medical device company headquartered in Wayne, Pennsylvania, with operations in Fall River, US. The company is a major provider of specialty medical devices for critical care and surgical procedures.

Teleflex Medical has received 39 FDA 510(k) clearances from 39 total submissions since 2003. The company maintains active regulatory engagement, with the latest clearance in 2025. Its cleared devices span multiple specialties including anesthesiology, general and plastic surgery, cardiovascular, and vascular access systems.

The company's product portfolio includes ligating clips, hemostatic devices, endotracheal tubes, intraosseous vascular access systems, and urethral catheters. These devices reflect Teleflex Medical's focus on surgical instrumentation and critical care solutions across diverse clinical settings.

Explore the complete list of device names, product codes, and individual clearance dates in the database to review Teleflex Medical's full regulatory history and specific device submissions.