Medical Device Manufacturer · MY , Ipoh, Perak, Darul Ridzuan

Kl-Kepong Rubber Products Sdn. Bhd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2003

Total

Cleared

Denied

Kl-Kepong Rubber Products Sdn. Bhd. has 3 FDA 510(k) cleared medical devices. Based in Ipoh, Perak, Darul Ridzuan, MY.

Latest FDA clearance: Jun 2025. Active since 2003. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Kl-Kepong Rubber Products Sdn. Bhd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.

Kl-Kepong Rubber Products Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kl-Kepong Rubber Products Sdn. Bhd.

3 devices

1-3 of 3

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 27, 2026