Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Centrix with 48 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2025: FluoroDose Varnish.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 21, 2025 | FluoroDose VarnishK250714 · LBH | 510(k) clearances |
| Oct 27, 2023 | Centrix FluoroSilver Silver Diamine Fluoride 38%K222459 · PHR | 510(k) clearances |
| Oct 15, 2020 | STATSTIXK200764 · MVL | 510(k) clearances |
| May 27, 2016 | NoCordK152826 · ELW | 510(k) clearances |
| Jul 8, 2014 | BENDA WEDGEK140144 · EJB | 510(k) clearances |
| Jul 25, 2012 | SENZZZZZ AWAYK120176 · LBH | 510(k) clearances |
| Jul 22, 2011 | RE / STASIS (TM) GINGIVAL RETRACTION PASTEK111348 · MVL | 510(k) clearances |
| Nov 4, 2009 | LIQUICORDK092384 · MVL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
