Medical Device Manufacturer · US , Shelton , CT

Centrix Incorporated - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2020

Total

Cleared

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.

FDA 510(k) cleared devices by Centrix Incorporated

1 devices

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