FDA device listing
actiTENS iOS app, actiTENS Android app, actiTENS standard kit, actiTENS spare, Charging Case spare,self-adhesive strip
FDA device listing 1738875747 · Stiplastics
Key facts
| Proprietary names | actiTENS iOS app, actiTENS Android app, actiTENS standard kit, actiTENS spare, Charging Case spare,self-adhesive strip |
|---|---|
| Owner/operator | Stiplastics |
| Owner/operator number | 10038835 |
| Product codes | GZJ, IPF, NGX, NYN |
| Device names | GZJ - Stimulator, Nerve, Transcutaneous, For Pain Relief, IPF - Stimulator, Muscle, Powered, NGX - Stimulator, Muscle, Powered, For Muscle Conditioning, NYN - Stimulator, Electrical, Transcutaneous, For Arthritis |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.5890, 890.5850 |
| Review panels | Neurology, Physical Medicine |
| Registered establishments | STIPLASTICS |
| Establishment registrations | 3009494725 |
| FEI numbers | 3009494725 |
| Establishment operations | Contract 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