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AUVON Red0510

by Shenzhen Yuwen E-Commerce Co., Ltd.

AUVON Red0510 is a Class II device made by Shenzhen Yuwen E-Commerce Co., Ltd., listed in FDA GUDID since 13 Nov 2023 (UDI-DI 06971292002468), 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 Number06971292002468 UDI-DI Date13 Nov 2023ListedStatusListed 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  • Withdrawn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
Transcutaneous electrical stimulation electrode, single-use
Model / reference
Red0510
Primary DI / UDI-DI
06971292002468
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
MRI safety
MR Safe

Related devices

Category: Transcutaneous electrical stimulation electrode, single-use

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

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

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

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)