FDA applicant

Konica Minolta Technoproduct Co., Ltd.

New York, NY1 decision2008–20080 recalls

FDA records 1 decision for Konica Minolta Technoproduct Co., Ltd. (New York, NY) in 2008: 1 510(k) clearance. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). Its devices cite 2 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, radiology panel, where it files most

How often FDA has decided Konica Minolta Technoproduct Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Konica Minolta Technoproduct Co., Ltd. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Konica Minolta Technoproduct 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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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 Medical and Graphic Corporation 1

Konica Minolta Technoproduct Co., Ltd.

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 “Konica”