Medical Device Manufacturer · US , Morrisville , NC

Teleflex Incorporated

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Teleflex Incorporated — FDA 510(k) Submissions

Teleflex Incorporated has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tube, Tracheal (w/wo Connector) . Use the specialty filter in the sidebar to narrow results.

1 devices
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All1 Anesthesiology 1