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CURA DIGITAL HEALTH SOLUTIONS INC

US

Last updated May 30, 2026

What CURA DIGITAL HEALTH SOLUTIONS INC makes

Cura Digital Health Solutions Inc manufactures reusable blood pressure cuffs designed for clinical and home monitoring. Their primary product, the Cura Blood Pressure Monitor, integrates with digital health platforms to provide automated readings and data tracking for patients and healthcare providers.

The company’s blood pressure cuffs fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to U.S. medical device compliance requirements.

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 Cura Digital Health Solutions Inc manufacture?

Cura Digital Health Solutions Inc specializes in reusable blood pressure cuffs. These devices are primarily designed for both clinical and home use, enabling continuous monitoring of blood pressure. Their focus is on integrating these cuffs with digital health platforms to streamline data collection and patient tracking.

Where is Cura Digital Health Solutions Inc based, and does this affect its regulatory compliance?

Cura Digital Health Solutions Inc is based in the United States. Since the company operates within the U.S., its devices must comply with U.S. medical device regulations, including those set by the FDA. This includes classification under FDA guidelines and potential listing in relevant databases like the UDI system.

Which regulatory registries or databases list Cura Digital Health Solutions Inc’s devices?

Cura Digital Health Solutions Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify device details and compliance status.

How are Cura Digital Health Solutions Inc’s blood pressure cuffs classified under medical device regulations?

Cura Digital Health Solutions Inc’s blood pressure cuffs fall under FDA Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

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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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
117540607

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Cura Blood Pressure Monitor TMB-1598-BS
FDA UDI
Class IIActive

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