510(k) Report

FDA applicant

Sagemax Bioceramics, Inc.

Federal Way, WA2 decisions2006–20140 recalls

FDA records 2 decisions for Sagemax Bioceramics, Inc. (Federal Way, WA) from 2006 to 2014: 2 510(k) clearances. All are in product code EIH (Powder, Porcelain). Its devices cite 6 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Sagemax Bioceramics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014: 1
2007high 1 (2014) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sagemax Bioceramics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EIHPowder, Porcelain2decisions

Whose devices does it build on?

Its devices cite 6 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 12 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K062695Sagemax Z-BlankSagemax Bioceramics, Inc. · 20068cite it
  • K130991Nexxzr (TM)T and Nexxzr (TM)SSagemax Bioceramics, Inc. · 20144cite it

What has FDA decided for it lately?

  • K130991Nexxzr (TM)T and Nexxzr (TM)SSagemax Bioceramics, Inc. · 2014
  • K062695Sagemax Z-BlankSagemax Bioceramics, Inc. · 2006

All 2 as Sagemax Bioceramics, Inc. →