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Ward 24/7 Aps

DK Last updated 22 Oct 2026 Part of Ward247 Aps

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Devices
1
Registries
FDA 510(k)
FDA recalls
0

Catalogue1

What Ward 24/7 Aps makes

Ward 24/7 Aps manufactures the WARD-CSS (v1.2.x), a continuous glucose monitoring (CGM) system designed for real-time blood glucose tracking and alerting. The device integrates with mobile applications to provide automated glucose readings and trend analysis for users with diabetes.

The WARD-CSS (v1.2.x) is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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 Ward 24/7 Aps manufacture?

Ward 24/7 Aps manufactures the WARD-CSS (v1.2.x), a continuous glucose monitoring (CGM) system. This device is specifically designed for real-time blood glucose tracking and provides automated glucose readings along with trend analysis. It is intended for users with diabetes to help monitor their glucose levels continuously.

Where is Ward 24/7 Aps based?

Ward 24/7 Aps is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the provided information.

Which regulatory registries list devices manufactured by Ward 24/7 Aps?

The WARD-CSS (v1.2.x) from Ward 24/7 Aps is listed in the FDA’s 510(k) clearance registry. This registry tracks medical devices that have undergone the FDA’s 510(k) premarket notification process, which is required for Class II devices to demonstrate substantial equivalence to a legally marketed predicate device.

How are devices from Ward 24/7 Aps classified under FDA regulations?

The WARD-CSS (v1.2.x) is classified as a Class II medical device under FDA regulations. Class II devices generally pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. The classification is determined based on factors like the device’s intended use, potential risks, and benefits.

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

Information

Country
DK