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VeriQuick 64410323

by Fourstar Group Inc.

VeriQuick 64410323 is a Class I device made by Fourstar Group Inc., listed in FDA GUDID since 11 Jun 2026 (UDI-DI 00049696676038), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00049696676038 UDI-DI Date11 Jun 2026ListedStatusListed 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  • Withdrawn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
VeriQuick
Generic name
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing
Model / reference
64410323
Primary DI / UDI-DI
00049696676038
FDA product code
NGA
GMDN term
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing
Device class
Class I
Regulation number
862.1300
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NGA (Test, Follicle Stimulating Hormone (Fsh), Over The Counter).

Other devices from Fourstar Group Inc.

See all devices from Fourstar Group Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)