510(k) Report

FDA applicant

Seo Han Corp., Ltd.

Daegu, KR1 decision1994–19940 recalls

FDA records 1 decision for Seo Han Corp., Ltd. (Daegu, KR) in 1994: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Seo Han Corp., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Seo Han Corp., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Seo Han Corp., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Seo Han Corp., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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