510(k) Report

FDA applicant

American Green Dent. Mfg, Inc.

Los Angeles, CA2 decisions2003–20040 recalls

FDA records 2 decisions for American Green Dent. Mfg, Inc. (Los Angeles, CA) from 2003 to 2004: 2 510(k) clearances. Most are in product codes EJH (Alloy, Metal, Base) and ELC (Scaler, Ultrasonic). 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 American Green Dent. Mfg, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Green Dent. Mfg, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — American Green Dent. Mfg, 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?

  • EJHAlloy, Metal, Base1decision
  • ELCScaler, Ultrasonic1decision

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.

  • K033044Dream Cleanse S Scaler, Dream Compact S ScalerAmerican Green Dent. Mfg, Inc. · 20041cites it

What has FDA decided for it lately?

  • K033044Dream Cleanse S Scaler, Dream Compact S ScalerAmerican Green Dent. Mfg, Inc. · 2004
  • K033045Dream Bond, Dreamcast Chrome, Dreamcast V, Dream Flexicast, Dream LithecastAmerican Green Dent. Mfg, Inc. · 2003

All 2 as American Green Dent. Mfg, Inc. →