Data / Medical devices / Handpiece, Direct Drive, Ac-Powered / Japan
FDA-registered makers of Handpiece, Direct Drive, Ac-Powered in Japan: 5 establishments
5 establishments in Japan are registered with the FDA to make Handpiece, Direct Drive, Ac-Powered (product code EKX). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Handpiece, Direct Drive, Ac-Powered
- Product code
- EKX
- Country
- Japan
Makers of Handpiece, Direct Drive, Ac-Powered in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| J. Morita MFG. Corp. | FUSHIMI-KU Kyoto, Japan | Manufacturer | 4 | October 11, 2018 | 0 | 0 | 0 | api.fda.gov |
| Nakanishi Inc. | Kanuma Tochigi, Japan | Manufacturer | 4 | September 12, 2013 | 0 | 0 | 0 | api.fda.gov |
| Force Engineering Co.ltd | Utsunomiya Tochigi, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Osada Electric Co., Ltd. | SHINAGAWA-KU Tokyo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanko Electronics Corporation | Midori Gunma, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.