Data / Medical devices / Locator, Acupuncture Point
Locator, Acupuncture Point (BWJ): 5 FDA-registered makers in 4 countries
5 establishments in 4 countries are registered with the FDA to make Locator, Acupuncture Point (product code BWJ, Class 2, 21 CFR 880.5580). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on February 26, 1980, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- BWJ
- Device class
- 2
- Regulation
- 880.5580
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| China | 2 |
| United States | 1 |
| India | 1 |
| Hong Kong | 1 |
Makers of Locator, Acupuncture Point
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 |
|---|---|---|---|---|---|---|---|---|
| Dragon Medical Co.,Ltd | Suzhou City Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Miridia Technology Inc. | Meridian, ID, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Chengmei Medical Products Company | NINGBO Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neurostimulation Medtech Private Limited | Chennai Tamil Nadu, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tens Plus Industrial Co. | Hong Kong, Hong Kong | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated February 26, 1980. 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.