Truabutment is one of 18433 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Truabutment - FDA 510(k) Cleared Devices
Recent clearances: TruAbutment DS, TruAbutment DS
2
Total
2
Cleared
0
Denied
Truabutment has 2 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Truabutment Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Withus Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Truabutment
2 devices