Teleflexmedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teleflexmedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rüsch Latex Gold Foley Catheter, Teleflex Rusch SoftSimplastic Foley Catheters, Sheridan Spiral-Flex Endotracheal Tubes
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) Regulatory Record - 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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