Altaviz, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Altaviz, LLC - FDA 510(k) Cleared Devices
Recent clearances: Altaviz Intravitreal Syringe, Altaviz Needle Kit II, Altaviz Needle Kit
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