Rubberex Alliance Sdn Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Rubberex Alliance Sdn Bhd - FDA 510(k) Cleared Devices
Recent clearances: Non-sterile Powder Free Nitrile Examination Gloves
1
Total
1
Cleared
0
Denied
Rubberex Alliance Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Ipoh, MY.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rubberex Alliance Sdn Bhd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Rubberex Alliance Sdn Bhd
1 devices