Medical Device Manufacturer · US , Irvine , CA

Altaviz, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

Altaviz, LLC has 3 FDA 510(k) cleared medical devices. Based in Irvine, US.

Latest FDA clearance: May 2025. Active since 2022. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Allied Regulatory Consulting as regulatory consultant.

FDA 510(k) Regulatory Record - Altaviz, LLC
3 devices
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All3 General Hospital 3