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Pixie Cup B0BFNLQC4L

by Pixie Cup, LLC

Pixie Cup B0BFNLQC4L, a transcutaneous electrical stimulation electrode (FDA Class II; FDA product code NUH, Stimulator, Nerve, Transcutaneous, Over-The-Counter) made by Pixie Cup, LLC, was listed in FDA GUDID on 9 Jan 2026 (UDI-DI 00850016867407); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850016867407 UDI-DI Date9 Jan 2026ListedStatusListed GUDID: not 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  • Withdrawn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
Pixie Cup
Generic name
Transcutaneous electrical stimulation electrode, reusable
Model / reference
B0BFNLQC4L
Primary DI / UDI-DI
00850016867407
FDA product code
NUH
GMDN term
Transcutaneous electrical stimulation electrode, reusable
Device class
Class II
Regulation number
882.5890
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

Other devices from Pixie Cup, LLC

See all devices from Pixie Cup, LLC →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)