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Pixie Cup M2506PC1915A

by Pixie Cup, LLC

Pixie Cup M2506PC1915A, a menstrual cup/disc (FDA Class II; FDA product code HHE, Cup, Menstrual) made by Pixie Cup, LLC, was listed in FDA GUDID on 25 Jun 2025 (UDI-DI 00715875074840); the registry lists it as not in commercial distribution (GUDID) as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00715875074840 UDI-DI Date25 Jun 2025ListedStatusListed 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  • Withdrawn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
Menstrual cup/disc, non-latex, reusable
Model / reference
M2506PC1915A
Primary DI / UDI-DI
00715875074840
FDA product code
HHE
GMDN term
Menstrual cup/disc, non-latex, reusable
Device class
Class II
Regulation number
884.5400
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HHE (Cup, Menstrual).

Other devices from Pixie Cup, LLC

See all devices from Pixie Cup, LLC →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)