Data / Medical devices / Hong Kong / Sostrong Industries Ltd.
Sostrong Industries Ltd.: FDA-registered device maker in Kwai Chung, Hong Kong, 2 510(k) clearances
Sostrong Industries Ltd. is registered with the FDA (registration 3002809311) in Kwai Chung, Hong Kong. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 12, 1992. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002809311
- Address
- Unit 8, 19/F Fook Yip Bldg. 53-57 Kwai Fung Crescent, Kwai Chung, Hong Kong, NA
- Owner or operator
- Sostrong Industries Ltd. (10081876)
- Roles
- Exporter to the US
- First device listed
- May 22, 2021
- Registered through
- 2026
- Brand names listed
- Alpha-Stim AID, Alpha-Stim M
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety | QJQ | 2 | Exporter to the US | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 12, 1992 | K903014 | ALPHA-STIM CS | QJQ | Substantially Equivalent | Electromedical Products, Inc. | accessdata.fda.gov |
| February 23, 1990 | K896948 | ALPHA-STIM CS | GZJ | Substantially Equivalent | Electromedical Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
Updated May 12, 1992. 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.