510(k) Report

FDA applicant

3D Global Biotech, Inc.

New Taipei City 221, TW2 decisions2019–20220 recalls

FDA records 2 decisions for 3D Global Biotech, Inc. (New Taipei City 221, TW) from 2019 to 2022: 2 510(k) clearances. All are in product code NXC (Aligner, Sequential). Its devices cite 2 predicates, 0 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 3D Global Biotech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2019: 12022: 1
2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — 3D Global Biotech, Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NXCAligner, Sequential2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 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.

  • K212803DailyMate Orthodontic Aligner System3D Global Biotech, Inc. · 20221cites it

What has FDA decided for it lately?

  • K212803DailyMate Orthodontic Aligner System3D Global Biotech, Inc. · 2022
  • K191774SmileAlign Orthodontic Aligner System3D Global Biotech, Inc. · 2019

All 2 as 3D Global Biotech, Inc. →