Precision Align, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Align, LLC - FDA 510(k) Cleared Devices
Recent clearances: Precision Align
1
Total
1
Cleared
0
Denied
Precision Align, LLC has 1 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Precision Align, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Evo820, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Precision Align, LLC
1 devices