Fora

FDA UDI

Class II (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name: FORA FDA UDI
Generic Name: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name: Blood Glucose Plus Blood Pressure Monitoring System FDA UDI
Model / Reference: D40g FDA UDI
Description: Blood Glucose Plus Blood Pressure Monitoring System FDA UDI

Identifiers

Primary DI / UDI-DI: 00816042013959 FDA UDI
510(k) Number: K101926 FDA UDI
FDA Product Code: NBW FDA UDI
DXN FDA UDI
GMDN Term: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 862.1345 FDA UDI
870.1130 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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Glucose monitoring system IVD, home-use

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

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Cleared under the same submission

K101926 also covers:

FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
FORA — FORA CARE INC.
GOJJI BLOOD PRESSURE WELCOME KIT — GOJJI, INC.

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 II	Pending data

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Manufacturer

Manufacturer: Fora Care Inc.

Sources (1)

FDA UDI aa2a58be-ea52-49a1-8a14-ab946cee5355 34 fields · synced May 30, 2026