PENTAMASTER MEDIQ SDN BHD is one of 201 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
PENTAMASTER MEDIQ SDN BHD - FDA 510(k) Cleared Devices
Recent clearances: MOWANA™ Auto Duo
1
Total
1
Cleared
0
Denied
PENTAMASTER MEDIQ SDN BHD has 1 FDA 510(k) cleared medical devices. Based in Simpang Ampat, MY.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by PENTAMASTER MEDIQ SDN BHD Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - PENTAMASTER MEDIQ SDN BHD
1 devices