Data / Medical devices / China / Jiangsu Maxf Electric Appliance Co.,ltd
Jiangsu Maxf Electric Appliance Co.,ltd: FDA-registered device maker in Changzhou City Jiangsu, China, 1 510(k) clearance
Jiangsu Maxf Electric Appliance Co.,ltd is registered with the FDA (registration 3017153262) in Changzhou City Jiangsu, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 26, 2023. 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
- 3017153262
- Address
- No.12 West District Road, Rulin Town Jintan District, Changzhou City Jiangsu, China, 213225
- Owner or operator
- Jiangsu MaxF Electric Appliance Co.,Ltd (10068621)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- April 9, 2020
- Registered through
- 2026
- Brand names listed
- Air Compression Therapy Device MF-AWI, Leg Massager, Air Compression Therapy Device MF-AWI, Massager, Air Compression Therapy Recovery System MF-AWI, Air Pressure Massager, Air Compression Therapy Recovery System MF-AWI, Air Pressure Massager., Infrared massage head,MF-IHM-01
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| October 26, 2023 | K230500 | Air Compression Therapy Recovery System (model: MF-AWI, MF-AWI.LED.A-801, MF-AWI.LED.B-801, MF-AWI.OLED.A-601, MF-AWI.LED.A-601, MF-AWI.LED.B-601, MF-AWI.OLED.A-401, MF-AWI.LED.A-401, MF-AWI.LED.B-401) | IRP | Substantially Equivalent | Jiangsu Maxf Electric Appliance Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Powered Inflatable Tube
- All makers of Massager, Therapeutic, Electric
- All makers of Lamp, Infrared, Therapeutic Heating
Updated October 26, 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.