AdvanTrode WWS3ET
AdvanTrode WWS3ET is a Class II device made by Pepin Manufacturing, Inc., cleared under FDA 510(k) K070807 on 23 May 2007 and listed in FDA GUDID since 5 Oct 2016 (UDI-DI 00677346310577), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00677346310577 | Date5 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK070807 | Date23 May 2007 | StatusActive |
Official records
- AccessGUDID record 00677346310577
- FDA 510(k) database K070807
Across registries
- FDA 510(k) K070807 decided 23 May 2007 Active
- FDA GUDID UDI-DI 00677346310577 listed 5 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K070807
- Listed FDA GUDID 00677346310577
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AdvanTrode
- Generic name
- Transcutaneous electrical stimulation electrode, single-use
- Model / reference
- WWS3ET
- Primary DI / UDI-DI
- 00677346310577
- 510(k) Number
- FDA product code
- GXY
- GMDN term
- Transcutaneous electrical stimulation electrode, single-use
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
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