510(k) Report

FDA applicant

Manufacturera Dental Continental

Laguna Niguel, CA2 decisions1999–20010 recalls

FDA records 2 decisions for Manufacturera Dental Continental (Laguna Niguel, CA) from 1999 to 2001: 2 510(k) clearances. Most are in product codes ELW (Material, Impression) and EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Manufacturera Dental Continental’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Manufacturera Dental Continental since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Manufacturera Dental Continental 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?

  • ELWMaterial, Impression1decision
  • EBIResin, Denture, Relining, Repairing, Rebasing1decision

What has FDA decided for it lately?

  • K011785Novel Print Cyan AlginatesManufacturera Dental Continental · 2001
  • K991577Nic Tone Acrylic ResinsManufacturera Dental Continental · 1999

All 2 as Manufacturera Dental Continental →