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FORA Control Solution (L1)

by Fora Care Inc. 4 variants

FORA Control Solution (L1) is a Class I device made by Fora Care Inc., listed in FDA GUDID since 27 Jun 2023 (UDI-DI 00816042014093), 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 Number00816042014093 UDI-DI Date27 Jun 2023ListedStatusListed 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  • Withdrawn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
Fora
Generic name
Total cholesterol lipid IVD, calibrator
Model / reference
Control Solution (L1)
Primary DI / UDI-DI
00816042014093
FDA product code
JJX
GMDN term
Total cholesterol lipid IVD, calibrator
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)).

Other devices from Fora Care Inc.

  • FORA P20v

    Class II
  • Fora 30g

    Class II
  • FORA Test N'GO Advance Pro

    Class II
  • FORA Small Size

    Class II

See all devices from Fora Care Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)