Tens Maker Wt-110
Tens Maker Wt-110 is a medical device (FDA Class II; FDA product code NUH, Stimulator, Nerve, Transcutaneous, Over-The-Counter) made by Hivox Biotek Inc., listed in FDA GUDID since 26 May 2021 (UDI-DI 04719880810000), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04719880810000 | Date26 May 2021 | StatusListed |
Official records
- AccessGUDID record 04719880810000
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Tens Maker
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / reference
- WT-110
- Primary DI / UDI-DI
- 04719880810000
- FDA product code
- NUH
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 882.5890
- GUDID distribution status
- In Commercial Distribution
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