FDA applicant

Modern Module, Inc.

Lncheon, KR1 decision2011–20110 recalls

FDA records 1 decision for Modern Module, Inc. (Lncheon, KR) in 2011: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

How often FDA has decided Modern Module, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Modern Module, Inc. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Modern”

FDA records each applicant name separately; these may or may not be the same firm.

Modern Medical Equipment Mfg., Ltd. 14 Modern Medical Equipment Manufacturing Limited 8 Modern Diagnostics, Inc. 5 Modern Rubber Industrial Co., Ltd. 5 Modern Healthcare Corp. 3 Modern Dental Laboratory (Dg) Co., Ltd. 2 Modern Materials 2 Modern Engineering Co., Inc. 2 Modern Medical Systems Co. 2 Modern Systems Technology, Inc. 2 Modern Medical Devices, Inc. 1 Modern Rubber Co., Ltd. C/O World Trade Svc. 1

Modern Module, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Modern”