510(k) Report

FDA applicant

Daeju Meditech Engineering Co., Ltd.

Seoul, KR3 decisions2021–20250 recalls

FDA records 3 decisions for Daeju Meditech Engineering Co., Ltd. (Seoul, KR) from 2021 to 2025: 3 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Since 2016 its 510(k)s took a median of 99 days from receipt to decision, against 90 for FDA’s reviews in the same codes and years. Its devices cite 3 predicates, 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2025

2021: 12024: 12025: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Daeju Meditech Engineering Co., Ltd. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Daeju Meditech Engineering Co., 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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