Teleflexmedical, Inc. - FDA 510(k) Cleared Devices
64
Total
61
Cleared
0
Denied
Teleflexmedical, Inc. has 61 FDA 510(k) cleared medical devices. Based in Jeffrey, US.
Latest FDA clearance: Aug 2024. Active since 1985. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Teleflexmedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Teleflexmedical, Inc.
64 devices
Cleared
Aug 01, 2024
Rüsch Latex Gold Foley Catheter
Gastroenterology & Urology
352d
Cleared
Jul 27, 2023
Teleflex Rusch SoftSimplastic Foley Catheters
Gastroenterology & Urology
755d
Cleared
Dec 06, 2019
Sheridan Spiral-Flex Endotracheal Tubes
Anesthesiology
101d
Cleared
Jul 01, 2019
Hudson RCI Voldyne Volumetric Exerciser
Anesthesiology
265d
Cleared
May 24, 2019
Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent Catheter
Gastroenterology & Urology
303d
Cleared
May 08, 2019
Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic...
Gastroenterology & Urology
145d
Cleared
Oct 12, 2018
Percuvance Percutaneous Surgical System
General & Plastic Surgery
93d
Cleared
Aug 02, 2018
Neonatal ConchaSmart Breathing Circuits
Anesthesiology
290d
Cleared
Feb 12, 2018
MiniLap System with MiniGrip Handle, MiniLap System with ThumbGrip Handle
Gastroenterology & Urology
151d
Cleared
May 05, 2017
Rusch Silicone Foley Catheter
Gastroenterology & Urology
311d
Cleared
Mar 17, 2017
UltraCath Continuous Nerve block Catheter
Anesthesiology
189d
Cleared
Feb 24, 2017
Rusch Simplastic Foley Catheters
Gastroenterology & Urology
120d
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