Asiga Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Asiga Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DentaTOOTH, Asiga DentaBASE
2
Total
2
Cleared
0
Denied
Asiga Pty, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Alexandria, AU.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Asiga Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pharmalex Pty, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Asiga Pty, Ltd.
2 devices