Data / Medical devices / Hong Kong / Hong Kong Etech Groups Limited
Hong Kong Etech Groups Limited: FDA-registered device maker in Hongkong, Hong Kong, 1 510(k) clearance
Hong Kong Etech Groups Limited is registered with the FDA (registration 3022929665) in Hongkong, Hong Kong. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3022929665
- Address
- Room 747,7/F,star House,3 Salisbury Road Tsim Sha Tsui, Hongkong, Hong Kong, 999077
- Owner or operator
- HONG KONG ETECH GROUPS LIMITED (10092912)
- Roles
- Manufacturer
- First device listed
- March 5, 2025
- Registered through
- 2026
- Brand names listed
- Humidifier, Massager, Red Light Sound Machine, Model: MA1189, Red Light Alarm Clock Speaker, Model: MA1156, Smart Cupping 30357, 30590, Transcutaneous Electrical Nerve Stimulator (9029SCM), fitness back stretcher (30907)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Manufacturer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Orthosis, Lumbar | IQE | 1 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 25, 2024 | K240292 | Transcutaneous Electrical Nerve Stimulator (9029SCM) | NUH | Substantially Equivalent | Hong Kong Etech Groups Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Orthosis, Lumbar
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Massager, Therapeutic, Electric
Updated March 25, 2024. 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.