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FORA CARE INC.

US

Last updated May 24, 2026

What FORA CARE INC. makes

The company manufactures in vitro diagnostics (IVDs) for glucose monitoring, including kits and control solutions for electrometry-based testing, as well as home-use systems for multiple clinical chemistry analytes. It also produces portable electronic sphygmomanometers for arm or wrist use, infrared ear thermometers, and benchtop nebulizers for delivering therapeutic agents. Glucose analysers for home monitoring are part of its portfolio, alongside glucose monitoring systems designed for self-testing.

The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States, where these devices are authorised for commercial distribution.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Fora Care Inc. manufacture?

Fora Care Inc. specialises in in vitro diagnostics (IVDs) and related monitoring devices. Its portfolio includes glucose monitoring solutions such as IVD kits, control solutions for electrometry-based testing, and home-use systems for analysing multiple clinical chemistry analytes. Additionally, the company produces portable electronic sphygmomanometers (blood pressure monitors for arm or wrist use), infrared ear thermometers, and benchtop nebulizers for delivering therapeutic agents. These devices are designed for both clinical and home-use settings.

Where is Fora Care Inc. based, and where are its devices authorised?

Fora Care Inc. is based in the United States. The company’s devices are authorised for commercial distribution in the US market, where they comply with applicable regulatory requirements. The portfolio includes products that fall under FDA classification, ensuring they meet the necessary standards for safety and performance.

Which regulatory registries or databases list Fora Care Inc.’s devices?

All of Fora Care Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This database is a centralised repository that tracks medical devices authorised for commercial distribution in the US, ensuring transparency and traceability of product information for regulatory and market oversight purposes.

How are Fora Care Inc.’s devices classified under FDA regulations?

Fora Care Inc.’s devices are classified under two categories: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve a higher level of risk and require special controls to ensure their safety and effectiveness. The classification depends on the device type, intended use, and potential health impact, as determined by FDA guidelines.

What kinds of glucose monitoring solutions does Fora Care Inc. offer?

Fora Care Inc. offers a range of glucose monitoring solutions tailored for both clinical and home-use settings. This includes glucose IVD kits and control solutions for electrometry-based testing, standalone glucose analysers designed for self-monitoring at home, and comprehensive glucose monitoring systems that integrate testing, data analysis, and user-friendly interfaces. These solutions cater to individuals managing diabetes or other conditions requiring frequent glucose monitoring.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
004340807

Catalogue (165)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
Fora Control Solution (L1)
FDA UDI
Class IActive
Fora D40d
FDA UDI
Class IIActive
Fora D40
FDA UDI
Class IIActive
Fora GTel/Test N'GO Advance/Test N'GO Advance Voice/Test N'GO Adv. Mobile
FDA UDI
Class IActive
Fora Test N'GO Advance Voice
FDA UDI
Class IIActive
Fora Test N'GO Advance Voice
FDA UDI
Class IActive
Fora Test N'GO Advance
FDA UDI
Class IIActive
Fora G20
FDA UDI
Class IIActive
Fora LANCING DEVICE
FDA UDI
Class IIActive
Fora VSM100 Pro
FDA UDI
Class IIActive
Fora VSM100 Pro
FDA UDI
Class IIActive
Fora TN'G/TN'G Voice
FDA UDI
Class IIActive
Fora IR20
FDA UDI
Class IIActive
Fora Test N'GO BP Mobile
FDA UDI
Class IIActive
Rosie RealTime
FDA UDI
Class IIActive
Fora V30/G30/Premium V10
FDA UDI
Class IIActive
Fora Control Solution (L1)
FDA UDI
Class IActive
Fora GTel/Test N'GO Advance/Test N'GO Advance Voice/Gojji
FDA UDI
Class IActive
SootheNeb NBL200
FDA UDI
Class IIActive
Fora Test N'GO Advance Voice
FDA UDI
Class IActive
Fora Control Solution (L1)
FDA UDI
Class IActive
Fora GTel
FDA UDI
Class IIActive
Fora Control Solution (Normal)
FDA UDI
Class IActive
Fora XL
FDA UDI
Class IIActive
ForaCare G30a
FDA UDI
Class IIActive
Fora Control Solution (Normal)
FDA UDI
Class IActive
Fora Control Solution (High)
FDA UDI
Class IActive
Fora Test N'GO Advance
FDA UDI
Class IActive
Fora IR42
FDA UDI
Class IIActive
SootheNeb NBL100
FDA UDI
Class IIActive
Fora Test N'GO Advance Voice
FDA UDI
Class IIActive
Fora IR20
FDA UDI
Class IIActive
Fora 30G STERILE LANCETS
FDA UDI
Class IIActive
Fora V30/G30/Premium V10
FDA UDI
Class IIActive
Fora Control Solution (L1)
FDA UDI
Class IActive
Fora 30G STERILE LANCETS
FDA UDI
Class IIActive
Fora GTel
FDA UDI
Class IIActive
Fora Test N'GO Advance Voice
FDA UDI
Class IIActive
Fora 30G SAFETY LANCET-ROUND
FDA UDI
Class IIActive
Fora TN'G Voice
FDA UDI
Class IIActive
Fora Control Solution (Normal)
FDA UDI
Class IActive
Fora TN'G Scale 550
FDA UDI
Class IActive
Fora Control Solution (L2)
FDA UDI
Class IActive
Fora SpO2
FDA UDI
Class IIActive
Fora D40 Pro
FDA UDI
Class IIActive
Fora Small Size
FDA UDI
Class IIActive
Fora IR20
FDA UDI
Class IIActive
Fora L1 Control Solution (FORA/gojji)
FDA UDI
Class IActive
Fora 6 Connect
FDA UDI
Class IActive
Fora P50
FDA UDI
Class IIActive

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