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Data / Medical devices / Massager, Therapeutic, Electric / Hong Kong

FDA-registered makers of Massager, Therapeutic, Electric in Hong Kong: 13 establishments

13 establishments in Hong Kong are registered with the FDA to make Massager, Therapeutic, Electric (product code ISA). 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
Massager, Therapeutic, Electric
Product code
ISA
Country
Hong Kong

Makers of Massager, Therapeutic, Electric in Hong Kong

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
China 1 Link, LtdMongkok Kowloon, Hong KongManufacturer0000api.fda.gov
Golden Aim International LtdShenzhen City,, GUANGDONG, CHINA, Hong KongContract manufacturer0000api.fda.gov
Gorgeous Beauty Equipment Manufacture LimitedHong Kong, Hong KongManufacturer0000api.fda.gov
Hebei Mita Biotechnology LimitedHong Kong, Hong KongManufacturer0000api.fda.gov
Hebei Mita Technology LimitedHong Kong, Hong KongManufacturer0000api.fda.gov
Hong Kong Etech Groups LimitedHongkong, Hong KongManufacturer0000api.fda.gov
Hong Kong Lute Technology Co., LimitedHong Kong, Hong KongForeign private label distributor, Manufacturer, Repackager or relabeler0000api.fda.gov
J&C Supply-Chains Trade LimitedHk, Hong KongManufacturer0000api.fda.gov
Mixen Company LimitedKowloon, Hong KongExporter to the US, Manufacturer0000api.fda.gov
Oman Medical Beauty Manufacture LimitedHong Kong, Hong KongManufacturer0000api.fda.gov
Tohkai Precision International Ltd.Kwun Tong, Kowloon, Hong KongManufacturer0000api.fda.gov
TVP Developments LtdKowloon, Hong KongExporter to the US, Specification developer0000api.fda.gov
Warrenslove(hongkong)limitedKowloon, Hong KongManufacturer0000api.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.