Medical Device Manufacturer · US , San Diego , CA

Vesalio, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2025
4
Total
3
Cleared
0
Denied

Vesalio, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Jan 2026. Active since 2025. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Vesalio, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Vesalio, Inc.

4 devices
1-4 of 4
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