Dasoft Partners is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dasoft Partners - FDA 510(k) Cleared Devices
Recent clearances: Advanced Dental Appliance, Advanced Dental Applicance
2
Total
2
Cleared
0
Denied
Dasoft Partners has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Last cleared in 2021. Active since 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dasoft Partners Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Aschwartz Consulting and J Blane, LLC.
FDA 510(k) Regulatory Record - Dasoft Partners
2 devices