Medical Device Manufacturer · US , Mchenry , IL

Centrix, Inc. - FDA 510(k) Cleared Devices

47 submissions · 47 cleared · Since 1979

Recent clearances: FluoroDose Varnish, Centrix FluoroSilver Silver Diamine Fluoride 38%

Total

Cleared

Denied

Centrix, Inc. has 47 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Latest FDA clearance: Nov 2025. Active since 1979.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Aztech Regulatory & Quality, LLC as regulatory consultant.

Centrix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Centrix, Inc.

47 devices

1-12 of 47

Centrix FluoroSilver Silver Diamine Fluoride 38%

RE / STASIS (TM) GINGIVAL RETRACTION PASTE

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Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Centrix, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Centrix, Inc.

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