FDA applicant

Dreamcon Co., Ltd.

Mission Viejo, CA1 decision2013–20130 recalls

FDA records 1 decision for Dreamcon Co., Ltd. (Mission Viejo, CA) in 2013: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 1 predicate, 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, ophthalmic panel, where it files most

How often FDA has decided Dreamcon Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Dreamcon Co., Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dreamcon Co., Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?