Data / Medical devices / China / Silverfox Corporation Limited
Silverfox Corporation Limited: FDA-registered device maker in Jiangmen Guangdong, China, 1 510(k) clearance
Silverfox Corporation Limited is registered with the FDA (registration 3014471045) in Jiangmen Guangdong, China. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 16, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014471045
- Address
- No.18, 1st TongLe Road, TangXia Town, Pengjiang District, Jiangmen Guangdong, China, 529000
- Owner or operator
- SILVERFOX CORPORATION LIMITED (10057491)
- Roles
- Manufacturer
- First device listed
- April 14, 2018
- Registered through
- 2026
- Brand names listed
- Electric treatment table, Electrical Wheelchair, Facial steamer, Isolation Mask, Treatment table, Trolley, beauty instrument, dental stool; stool and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Manufacturer | accessdata.fda.gov |
| Chair And Table, Medical | KMN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Device, Patient Transfer, Powered | FRZ | 2 | Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Suit, Surgical | FXO | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| September 16, 2022 | K221799 | Electric Wheelchair, Model: 9000N | ITI | Substantially Equivalent | Silver Fox Corporation Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Accessory, Surgical Apparel
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Device, Patient Transfer, Powered
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Chair And Table, Medical
- All makers of Chair, Examination And Treatment
Updated September 16, 2022. 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.