Data / Medical devices / Device, Acupressure
Device, Acupressure (MVV): 8 FDA-registered makers in 4 countries
8 establishments in 4 countries are registered with the FDA to make Device, Acupressure (product code MVV, Class U). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 13 510(k) clearances under this code, the latest on June 29, 2022, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MVV
- Device class
- U
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| China | 4 |
| United States | 2 |
| Hong Kong | 1 |
| United Kingdom | 1 |
Makers of Device, Acupressure
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 |
|---|---|---|---|---|---|---|---|---|
| Apothecary Products, LLC. | Burnsville, MN, United States | Repackager or relabeler, Specification developer | 2 | November 26, 2004 | 0 | 0 | 0 | api.fda.gov |
| Vastrade Manufacturing Corporation | Shenzhen Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | 2 | November 26, 2004 | 0 | 0 | 0 | api.fda.gov |
| FridaBaby LLC | Miami, FL, United States | Complaint file establishment, Specification developer | 1 | June 29, 2022 | 0 | 0 | 0 | api.fda.gov |
| Hopstech Industries Ltd | Kwun Tong, Kowloon, Hong Kong, Hong Kong | Manufacturer | 1 | July 26, 2007 | 0 | 0 | 0 | api.fda.gov |
| Sea-Band, Ltd. | Hinckley, Leicestershire, United Kingdom | Manufacturer | 1 | January 7, 2004 | 0 | 0 | 0 | api.fda.gov |
| Shijiazhuang Aofeite Medical Device Co.,Ltd | Shijiazhuang Hebei, China | Exporter to the US, Manufacturer | 1 | September 1, 2021 | 0 | 0 | 0 | api.fda.gov |
| Tung Hing Plastic & Metal(shenzhen) Co. Ltd. | LONGGANG DIST, SHENZHEN Guangdong, China | Manufacturer | 1 | November 26, 2004 | 0 | 0 | 0 | api.fda.gov |
| Dongguan Sheng Yan Industrial Co., Ltd. | DongGuan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 29, 2022. 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.