FDA device listing
Electromagnetic Stimulation System Models:ES01,ES02,ES03,EMS Device Models:EMS01,EMS02,EMS03,Home Massage Device…
FDA device listing 1142068359 · WUHAN ZJZK TECHNOLOGY CO.,LTD. (aka WUHAN ZJKC TECHNOLOGY CO
Key facts
| Proprietary names | Electromagnetic Stimulation System Models:ES01,ES02,ES03,EMS Device Models:EMS01,EMS02,EMS03,Home Massage Device Models:HM01,HM02,HM03,Nerve Stimulator Device Models:NS01,NS02,NS03,Shockwave Therapy Machine Models:ST01,ST02,ST02,Tens Device Models:TENS01,TENS02,TENS03 |
|---|---|
| Owner/operator | WUHAN ZJZK TECHNOLOGY CO.,LTD. (aka WUHAN ZJKC TECHNOLOGY CO |
| Owner/operator number | 10093038 |
| Product codes | ISA |
| Device names | ISA - Massager, Therapeutic, Electric |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5660 |
| Review panels | Physical Medicine |
| Registered establishments | WUHAN ZJZK TECHNOLOGY CO.,LTD. (AKA WUHAN ZJKC TECHNOLOGY CO.,LTD.) |
| Establishment registrations | 3015338588 |
| FEI numbers | 3015338588 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database