FDA applicant

Konica Minolta Sensing, Inc.

Denver, CO3 decisions2001–20062 recalls

FDA records 3 decisions for Konica Minolta Sensing, Inc. (Denver, CO) from 2001 to 2006: 3 510(k) clearances. All are in product code DQA (Oximeter). Its devices cite 3 predicates, 1 of them its own earlier devices. 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Konica Minolta Sensing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Konica Minolta Sensing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Konica Minolta Sensing, 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?

What has been recalled?

Other applicant names beginning “Konica”