Medical Device Manufacturer · US , Palo Alto , CA

Viz. Ai, Inc. - FDA 510(k) Cleared Devices

11 submissions · 10 cleared · Since 2018

Total

Cleared

Denied

Viz. Ai, Inc. has 10 FDA 510(k) cleared radiology devices. Based in Palo Alto, US.

Latest FDA clearance: Jun 2025. Active since 2018.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Viz. Ai, Inc.

11 devices

1-11 of 11

Cleared Jun 10, 2025

Viz Subdural+, Viz SUBDURAL PLUS

K250354 · QIH

Radiology · 123d

Cleared Feb 05, 2024

Viz HDS, Viz Volume Plus, Viz ICH+

K232363 · QIH

Radiology · 182d

Not Cleared Aug 03, 2023

Viz HCM

DEN230003 · QXO

Cardiovascular · 205d

Viz ANEURYSM, Viz ANX

Viz. Ai, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Viz. Ai, Inc.

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