Data / Medical devices / China / XF Agencija Limited
XF Agencija Limited: FDA-registered device maker in Wanchai Hong Kong, China, 1 510(k) clearance
XF Agencija Limited is registered with the FDA (registration 3026322014) in Wanchai Hong Kong, China. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 2, 2019. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3026322014
- Address
- Room 1502,Beverly House,93-107 Lockhart Road, Wanchai Hong Kong, China, 999077
- Owner or operator
- XF Agencija Limited (10087132)
- Roles
- Specification developer
- First device listed
- January 16, 2023
- Registered through
- 2026
- Brand names listed
- Nooro Foot Massager, Nooro Knee Massager, Nooro Whole Body Massager
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 2, 2019 | K190009 | Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) | NUH | Substantially Equivalent | Hong Qiangxing (Shenzhen) Electronics Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Massager, Therapeutic, Electric
- All makers of Massager, Therapeutic, Manual
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
Updated December 2, 2019. 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.