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Pixie Cup B09NQDYZMW

by Pixie Cup, LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850016867209 UDI-DI Date5 Nov 2025ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 blood irradiation laser
Model / Reference
B09NQDYZMW
Primary DI / UDI-DI
00850016867209
FDA Product Code
NUH
GMDN Term
Transcutaneous blood irradiation laser
Device Class
Class II
Regulation Number
882.5890
GUDID distribution status
In Commercial Distribution

Other devices from Pixie Cup, LLC

See all devices from Pixie Cup, LLC →

Properties

  • Lot / Batch Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No