Centrix Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centrix Incorporated - FDA 510(k) Cleared Devices
Recent clearances: STATSTIX
1
Total
1
Cleared
0
Denied
Centrix Incorporated has 1 FDA 510(k) cleared medical devices. Based in Shelton, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Centrix Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medtek, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Centrix Incorporated
1 devices