510(k) Report

FDA applicant

GreenMark Biomedical, Inc.

East Lansing, MI2 decisions2021–20250 recalls

FDA records 2 decisions for GreenMark Biomedical, Inc. (East Lansing, MI) from 2021 to 2025: 2 510(k) clearances. Most are in product codes LFC (Device, Caries Detection) and LBH (Varnish, Cavity). 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 GreenMark Biomedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2021: 12025: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — GreenMark Biomedical, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LFCDevice, Caries Detection1decision
  • LBHVarnish, Cavity1decision

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.

  • K200601LumiCare Caries Diagnostic RinseGreenMark Biomedical, Inc. · 20211cites it

What has FDA decided for it lately?

  • K241568CrystLCare™ PRO Biorestorative, Fluoride-PlusGreenMark Biomedical, Inc. · 2025
  • K200601LumiCare Caries Diagnostic RinseGreenMark Biomedical, Inc. · 2021

All 2 as GreenMark Biomedical, Inc. →