Teleflex Medical Sdn. Bhd. is one of 75 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Teleflex Medical Sdn. Bhd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Teleflex Medical Sdn. Bhd. has 2 FDA 510(k) cleared medical devices. Based in Kamunting, MY.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Teleflex Medical Sdn. Bhd. Filter by specialty or product code using the sidebar.
Teleflex Medical Sdn. Bhd. — FDA 510(k) Products and Clearance History
2 devices
Cleared
May 15, 2026
Iso-Gard Filter Straight
General Hospital
267d
Cleared
Jan 20, 2026
Rusch SoftSimplastic Foley Catheters
Gastroenterology & Urology
161d