Data / Medical devices / Toothbrush, Ionic, Battery-Powered
Toothbrush, Ionic, Battery-Powered (MMD): 22 FDA-registered makers in 8 countries
22 establishments in 8 countries are registered with the FDA to make Toothbrush, Ionic, Battery-Powered (product code MMD, Class 1, 21 CFR 872.6865). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on June 24, 1997, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Product code
- MMD
- Device class
- 1
- Regulation
- 872.6865
- Medical specialty
- Dental
Makers by country
| Country | Makers |
|---|---|
| China | 13 |
| Japan | 2 |
| Taiwan | 2 |
| South Korea | 1 |
| United Kingdom | 1 |
| United States | 1 |
| Thailand | 1 |
| Hong Kong | 1 |
Makers of Toothbrush, Ionic, Battery-Powered
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| IONIC Corporation | Nagareyama Chiba, Japan | Exporter to the US, Manufacturer | 1 | March 4, 1994 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Ainengke Electronics Co, Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | June 24, 1997 | 0 | 0 | 0 | api.fda.gov |
| BSD Product Design Inc. | Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Conquer Industry Co., Limited | Wenzhou Zhejiang, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DayOn Daily Chemical Co., Ltd | Yangzhou Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fourstar Group Inc. | Taipei, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hansung Company | Gimpo-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Bailu Brushes Co., Ltd | YANGZHOU Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Province Yangzhou Shuguang Toothbrush Manufactory | YANG ZHOU Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Jianjie Daily And Cosmetics Co., Ltd. | Cixi Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ordo Club Limited | Altrincham, Cheshire Trafford, United Kingdom | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pak Mane Plastic And Metal (Shen Zhen) Company Limited | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rosemarie Products Company, LLC | Mason, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Shift Electrics Co.,ltd. | Shanghai, China | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Relish Technology Co.,ltd | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shift Technology (thailand) Co., Ltd. | Amphur Phan Thong Chon Buri, Thailand | Complaint file establishment, Contract manufacturer, Exporter to the US | 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 | |
| Truly Instrument Limited | Kwai Chung, Hong Kong | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Twinklers Limited | SHENZHEN Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xiamen Jieboya Technology Co.ltd | Xiamen Fujian, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yangzhou Royal Home Products Manufacture Co., Ltd. | Yangzhou Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yangzhou Xintaiyang Plastic Daily Chemical Co., Ltd. | Yangzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 24, 1997. 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.