Fora

FDA UDI

Class I (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name: FORA FDA UDI
Generic Name: Uric acid IVD, reagent FDA UDI
Device Name: Uric Acid Test Strip FDA UDI
Model / Reference: 6 Connect FDA UDI
Description: Uric Acid Test Strip FDA UDI

Identifiers

Primary DI / UDI-DI: 00816042014116 FDA UDI
FDA Product Code: LFQ FDA UDI
GMDN Term: Uric acid IVD, reagent FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.1775 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Uric acid IVD, reagent

Fora by Fora Care Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

URIC ACID REAGENT KIT（URICASE METHOD） — DIRUI INDUSTRIAL CO., LTD · IVD General
BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
Uric Acid (UA) — Maccura Biotechnology Co., Ltd. · IVD General
Liquick Cor-UA 120 — PZ CORMAY Spółka Akcyjna · IVD General
URIC ACID Kit — KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ · IVD General
BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
JAS Diagnostics — Drew Scientific , Ltd. · Class I
Uric acid — Kalians Corporation · IVD General

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Fora Care Inc.

Sources (1)

FDA UDI a07fc021-80b7-48c2-b6c9-095bee5a7ce2 33 fields · synced May 30, 2026