FDA applicant

Konica Medical and Graphic Corporation

Mie-Ken, JP1 decision2003–20030 recalls

FDA records 1 decision for Konica Medical and Graphic Corporation (Mie-Ken, JP) in 2003: 1 510(k) clearance. All are in product code LMC (Camera, Multi Format, Radiological). 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 Konica Medical and Graphic Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Konica Medical and Graphic Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Konica Medical and Graphic Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Konica”

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

Konica Minolta Medical & Graphic, Inc. 27 Konica Minolta, Inc. 25 Konica Medical Corp. 12 Konica Minolta Healthcare Americas, Inc. 6 Konica Corp. 5 Konica Minolta Sensing, Inc. 3 Konica Minolta Technoproduct Co., Ltd. 1

Konica Medical and Graphic Corporation

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Konica”