Medical Device Manufacturer · MY , Kamunting

Teleflex Medical Sdn. Bhd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026
1
Total
1
Cleared
0
Denied

Teleflex Medical Sdn. Bhd. has 1 FDA 510(k) cleared medical devices. Based in Kamunting, MY.

Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Teleflex Medical Sdn. Bhd. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Teleflex Medical Sdn. Bhd.

1 devices
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