FDA applicant

Konica Corp.

New York, NY5 decisions1992–19990 recalls

FDA records 5 decisions for Konica Corp. (New York, NY) from 1992 to 1999: 5 510(k) clearances. Most are in product codes LMC (Camera, Multi Format, Radiological) and KPR (System, X-Ray, Stationary). 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 Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Konica Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Konica Corp. 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 Minolta Sensing, Inc. 3 Konica Medical and Graphic Corporation 1 Konica Minolta Technoproduct Co., Ltd. 1

Konica Corp.

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”