Data / Medical devices / Hong Kong / Green Island International TCM Group Limited
Green Island International TCM Group Limited: FDA-registered device maker in Hk, Hong Kong, 1 510(k) clearance
Green Island International TCM Group Limited is registered with the FDA (registration 3010813366) in Hk, Hong Kong. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3010813366
- Address
- Shop A10-A11, G/F, Koon Wah Building, No.2, Yuen Shun Circuit, Yuen Chau Kok, NT, Hk, Hong Kong, 999077
- Owner or operator
- Green Island International TCM Group Limited (10078752)
- Roles
- Specification developer
- First device listed
- November 3, 2020
- Registered through
- 2026
- Brand names listed
- Foot Pad Electrode, Cupping Electrode, Point Electrode, Silicone Cupping Set
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Specification developer | accessdata.fda.gov |
| Electrode, Cutaneous | GXY | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| December 19, 2023 | K221199 | Conductive Silicone Electrode (model: Foot Pad Electrode, Cupping Electrode, Point Electrode) | GXY | Substantially Equivalent | Green Island International Tcm Group Limited | accessdata.fda.gov |
Compare with other makers
Updated December 19, 2023. 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.