FDA applicant

DentMedi Co., Ltd.

Gunposi, KR1 decision2026–20260 recalls

FDA records 1 decision for DentMedi Co., Ltd. (Gunposi, KR) in 2026: 1 510(k) clearance. All are in product code EIH (Powder, Porcelain). 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 DentMedi Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

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DentMedi Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?