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Lia Pregnancy Test 2 Pack

by Lia Diagnostics

Lia Pregnancy Test 2 Pack is a Class II device made by Lia Diagnostics, listed in FDA GUDID since 15 Mar 2021 (UDI-DI 00860000380621), 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 Number00860000380621 UDI-DI Date15 Mar 2021ListedStatusListed 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  • Withdrawn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
Lia Pregnancy Test
Generic name
Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, clinical
Model / reference
2 Pack
Primary DI / UDI-DI
00860000380621
FDA product code
LCX
GMDN term
Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, clinical
Device class
Class II
Regulation number
862.1155
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter).

Other devices from Lia Diagnostics

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
Other properties (12, all answered No)