See-Mode Technologies Pte, Ltd. is one of 29 FDA 510(k) medical device manufacturers from Singapore in the dataset, ranked by real submission volume.
See-Mode Technologies Pte, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: See-Mode Augmented Reporting Tool, Thyroid (SMART-T), AVA (Augmented Vascular Analysis)
2
Total
2
Cleared
0
Denied
See-Mode Technologies Pte, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Singapore, SG.
Latest FDA clearance: Sep 2024. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by See-Mode Technologies Pte, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Matrix Medical Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - See-Mode Technologies Pte, Ltd.
2 devices