Clearadvance, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clearadvance, LLC - FDA 510(k) Cleared Devices
Recent clearances: Titan Dental Design
1
Total
1
Cleared
0
Denied
Clearadvance, LLC has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2023. Active since 2023. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Clearadvance, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.
FDA 510(k) Regulatory Record - Clearadvance, LLC
1 devices