FDA applicant

Nsk Nakanishi, Inc.

Tochigi-Ken, JP13 decisions1996–19991 recall

FDA records 13 decisions for Nsk Nakanishi, Inc. (Tochigi-Ken, JP) from 1996 to 1999: 13 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EBW (Controller, Foot, Handpiece And Cord). 1 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Nsk Nakanishi, Inc. since 2007.

Recalls per year

1in 2016

2007high 1 (2016) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Nsk Nakanishi, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Nsk Nakanishi, Inc.

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?

What has been recalled?