Centrix, Inc.
FDA 510(k) & PMA Approved Devices — 46 products
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Total Devices46
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250714 | FluoroDose Varnish | LBH | 2025-11-21 | View |
| 510(k) | K222459 | Centrix FluoroSilver Silver Diamine Fluoride 38% | PHR | 2023-10-27 | View |
| 510(k) | K152826 | NoCord | ELW | 2016-05-27 | View |
| 510(k) | K120176 | SENZZZZZ AWAY | LBH | 2012-07-25 | View |
| 510(k) | K111348 | RE / STASIS (TM) GINGIVAL RETRACTION PASTE | MVL | 2011-07-22 | View |
| 510(k) | K092384 | LIQUICORD | MVL | 2009-11-04 | View |
| 510(k) | K091380 | CORDCAP | MVL | 2009-07-30 | View |
| 510(k) | K021131 | CHLORAPREP | LBH | 2002-09-26 | View |
| 510(k) | K021146 | D/SENSE 1-STEP | EJK | 2002-07-02 | View |
| 510(k) | K010133 | VERSALUX | EBZ | 2001-04-05 | View |
| 510(k) | K001050 | CALCIJECT | EJK | 2000-07-21 | View |
| 510(k) | K992629 | D/SENSE II (GREEN-OR) DENTIN DESENSITIZER | LBH | 1999-10-22 | View |
| 510(k) | K981972 | GREEN-OR DENTIN DESENSITIZER | LBH | 1998-12-07 | View |
| 510(k) | K982665 | JUMBO SILVER-REINFORCED GLASS IONOMER | EMA | 1998-09-08 | View |
| 510(k) | K980568 | JUMBO GLASS IONOMER CEMENT | EMA | 1998-04-30 | View |
| 510(k) | K973285 | D/SENSE-T | KLE | 1998-02-25 | View |
| 510(k) | K973257 | VERSAETCH | EBF | 1997-11-17 | View |
| 510(k) | K971121 | ENCORE BOND | KLE | 1997-06-27 | View |
| 510(k) | K965138 | DENTINSENSE B/C | KLE | 1997-02-14 | View |
| 510(k) | K964735 | DENTINSENSE | KLE | 1997-02-05 | View |
No matching devices.
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