Skip to content

Auvon TU2424

by Shenzhen Yuwen E-Commerce Co., Ltd. 3 variants

Auvon TU2424 is a Class II device made by Shenzhen Yuwen E-Commerce Co., Ltd., listed in FDA GUDID since 17 Dec 2025 (UDI-DI 06971292004295), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971292004295 UDI-DI Date17 Dec 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Auvon
Generic name
Analgesic transcutaneous electrical nerve stimulation system
Model / reference
TU2424
Primary DI / UDI-DI
06971292004295
FDA product code
NUH, NGX
GMDN term
Analgesic transcutaneous electrical nerve stimulation system
Device class
Class II
Regulation number
882.5890, 890.5850
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter).

Other devices from Shenzhen Yuwen E-Commerce Co., Ltd.

See all devices from Shenzhen Yuwen E-Commerce Co., Ltd. →

Properties

  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)