Jentera Jaya Sdn Bhd is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jentera Jaya Sdn Bhd - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Jentera Jaya Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in San Luis Opispo, US.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Jentera Jaya Sdn Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jentera Jaya Sdn Bhd
1 devices