510(k) Report

FDA applicant

Micro Dental Laboratories

Dublin, CA3 decisions1998–19990 recalls

FDA records 3 decisions for Micro Dental Laboratories (Dublin, CA) from 1998 to 1999: 3 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EHP (Clasp, Preformed). 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 Micro Dental Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micro Dental Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micro Dental Laboratories 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?

  • EBIResin, Denture, Relining, Repairing, Rebasing1decision
  • EHPClasp, Preformed1decision
  • EJTAlloy, Gold-Based Noble Metal1decision

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.

  • K980613Progold Electrocoping SystemMicro Dental Laboratories · 19981cites it

What has FDA decided for it lately?

  • K984467FusicrylMicro Dental Laboratories · 1999
  • K980613Progold Electrocoping SystemMicro Dental Laboratories · 1998
  • K974622Dental DMicro Dental Laboratories · 1998

All 3 as Micro Dental Laboratories →