Data / Medical devices / United States / Everyway4all
Everyway4all: FDA-registered device maker in Chino, CA, United States, 3 510(k) clearances
Everyway4all is registered with the FDA (registration 3011267903) in Chino, CA, United States. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 16, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011267903
- Address
- 14636 Central Ave, Chino, CA, United States, 91710
- Owner or operator
- EVERYWAY4ALL (10053071)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- December 22, 2016
- Registered through
- 2026
- Brand names listed
- EM-5200, EM-6300A Premier Combo Plus, EM-6300P, EM-6300P Premier Combo Plus, EV-804, EV-805, EV-806, EV-820 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Repackager or relabeler | 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 16, 2015 | K151479 | EV-820 OTC Pain Relief TENS | NUH | Substantially Equivalent | Everyway Medical Instruments Co.,Ltd | accessdata.fda.gov |
| August 3, 2009 | K083302 | LIFECARE ELECTRODES | GXY | Substantially Equivalent | Everyway Medical Instruments Co.,Ltd | accessdata.fda.gov |
| September 5, 2007 | K071951 | COMFY SERIES: EV-804, EV-805 & EV-806 | GZJ | Substantially Equivalent | Everyway Medical Instruments Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Electrode, Cutaneous
- All makers of Stimulator, Muscle, Powered
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
Updated October 16, 2015. 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.