Data / Medical devices / Toothbrush, Manual / Japan
FDA-registered makers of Toothbrush, Manual in Japan: 11 establishments
11 establishments in Japan are registered with the FDA to make Toothbrush, Manual (product code EFW). 0 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
- Toothbrush, Manual
- Product code
- EFW
- Country
- Japan
Makers of Toothbrush, Manual in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aitec Co., Ltd. | OZU-SHI Ehime, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentalpro Co., Ltd. | YAO-SHI Osaka, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fine Company Ltd. | Iga Mie, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hokubi Co.,ltd. | Nonoichi Ishikawa, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lion Corporation | Taito-ku Tokyo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nishiwaki Industrial Co., Ltd. | Yao, Osaka, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nishio Co., Ltd | Chiba, Japan | Foreign private label distributor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sato Pharmaceutical Co., Ltd. | MINATO-KU Tokyo, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shiken Co.,ltd. | Osaka, Japan | Exporter to the US, Foreign private label distributor, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shinnnichi Corporation Co.,ltd | Higashi-Osaka, Japan | Exporter to the US, Foreign private label distributor, Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vivatec Co.,ltd. | Sakai-shi Osaka, Japan | Contract manufacturer, 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.